FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Nico Leschot

Research Profile

Physiology

Procedures

Disorders

Occupations

Genetic Counseling

Geographic Areas

Netherlands

Living Beings

Concepts & Ideas

Anatomy

X Chromosome

Co-author Network

Publications

TOP 3
Fleur Vansenne; P M M Bossuyt; K Gerssen-Schoorl; Mariette Goddijn; H Lemmink; Nico J Leschot; Bert Redeker; S Snijder; Fulco van der Veen; Corianne De Borgie
Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality.
S M Schade van Westrum; Anthonie J van Essen; A A M Wilde; Egbert Bakker; R J de Haan; Marianne De Visser; L Dekker; Edo M Hoogerwaard; P F Ippel; Nico J Leschot; D F Majoor-Krakauer; Jan C Oosterwijk; T S Standaar; Anneke J van der Kooi
Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy.
M T M Franssen; Mariette Goddijn; P M M Bossuyt; Nico J Leschot; A M Musters; Sjoerd Repping; Fulco van der Veen; Johanna C Korevaar
Reproductive outcome after PGD in couples with recurrent miscarriage carrying a structural chromosome abnormality: a systematic review.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Nico Leschot (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2011: Fleur Vansenne; P M M Bossuyt; K Gerssen-Schoorl; Mariette Goddijn; H Lemmink; Nico J Leschot; Bert Redeker; S Snijder; Fulco van der Veen; Corianne De Borgie
Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality.
Reproductive biomedicine online 2011;23(4):525-33.
2011: S M Schade van Westrum; Anthonie J van Essen; A A M Wilde; Egbert Bakker; R J de Haan; Marianne De Visser; L Dekker; Edo M Hoogerwaard; P F Ippel; Nico J Leschot; D F Majoor-Krakauer; Jan C Oosterwijk; T S Standaar; Anneke J van der Kooi
Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy.
Neurology 2011;77(1):62-6.
2011: M T M Franssen; Mariette Goddijn; P M M Bossuyt; Nico J Leschot; A M Musters; Sjoerd Repping; Fulco van der Veen; Johanna C Korevaar
Reproductive outcome after PGD in couples with recurrent miscarriage carrying a structural chromosome abnormality: a systematic review.
Human reproduction update 2011;17(4):467-75.
2011: Emmy Van Den Boogaard; Rosella P M G Hermens; Nico J Leschot; Ruth Baron; Jos H A Vollebergh; Rob E Bernardus; Fulco van der Veen; Jan A M Kremer; Mariëtte Goddijn
Identification of barriers for good adherence to a guideline on recurrent miscarriage.
Acta obstetricia et gynecologica Scandinavica 2011;90(2):186-91.
2010: Anna M Musters; Moniek Twisk; Nico J Leschot; Cor Oosterwijk; Johanna C Korevaar; Sjoerd Repping; Fulco van der Veen; Mariette Goddijn
Perspectives of couples with high risk of transmitting genetic disorders.
Fertility and sterility 2010;94(4):1239-43.
2010: E van den Boogaard; S P Kaandorp; M T M Franssen; Ben Mol; Nico J Leschot; Cokkie H Wouters; Fulco van der Veen; Johanna C Korevaar; Mariette Goddijn
Consecutive or non-consecutive recurrent miscarriage: is there any difference in carrier status?
Human reproduction (Oxford, England) 2010;25(6):1411-4.
2010: Fleur Vansenne; Corianne De Borgie; Johanna C Korevaar; Maureen T M Franssen; Eva Pajkrt; Kerstin B M Hansson; Nico J Leschot; Patrick M M Bossuyt; Fulco van der Veen; Mariëtte Goddijn
Low uptake of prenatal diagnosis after established carrier status of a balanced structural chromosome abnormality in couples with recurrent miscarriage.
Fertility and sterility 2010;94(1):296-300.e1-3.
2010: E van den Boogaard; Mariette Goddijn; Nico J Leschot; F van der Veen; J A M Kremer; R P M G Hermens
Development of guideline-based quality indicators for recurrent miscarriage.
Reproductive biomedicine online 2010;20(2):267-73.
2009: Jet Bliek; Marielle Alders; Saskia M Maas; Roelof-Jan Oostra; Deborah M Mackay; Karin van der Lip; Johnatan L Callaway; Alice Brooks; Sandra van 't Padje; Andries Westerveld; Nico J Leschot; marcel mannens
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.
European journal of human genetics : EJHG 2009;17(12):1625-34.
2008: ED Mollema; Ellen M A Smets; M E Richard; A M Schiphorst; Nico J Leschot
Psycho-social counselling in predictive genetic testing for cancer: the association between number of supportive sessions and client characteristics as assessed by psycho-social workers.
Journal of genetic counseling 2008;17(5):480-8.
2008: M T M Franssen; Johanna C Korevaar; W M Tjoa; Nico J Leschot; Patrick Bossuyt; Alida C Knegt; R F Suykerbuyk; Ron Hochstenbach; Fulco van der Veen; Mariette Goddijn
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.
Prenatal diagnosis 2008;28(5):408-11.
2007: Cora M Aalfs; Frans J Oort; J C J M de Haes; Nico J Leschot; Ellen M A Smets
A comparison of counselee and counselor satisfaction in reproductive genetic counseling.
Clinical genetics 2007;72(2):74-82.
2007: Nico J Leschot; Arthur A M Wilde
[The optimal treatment of chronic heart failure with beta-blockers may be dependent upon the genetic background of the patient].
Nederlands tijdschrift voor geneeskunde 2007;151(29):1610-1.
2007: M T M Franssen; Johanna C Korevaar; Fulco van der Veen; kees boer; Nico J Leschot; Mariette Goddijn
Management of recurrent miscarriage: evaluating the impact of a guideline.
Human reproduction (Oxford, England) 2007;22(5):1298-303.
2007: M T M Franssen; Johanna C Korevaar; Nico J Leschot; Patrick Bossuyt; Alida C Knegt; Klasien B J Gerssen-Schoorl; Cokkie H Wouters; K B M Hansson; P F R Hochstenbach; Kamlesh Madan; Fulco van der Veen; Mariette Goddijn
[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping].
Nederlands tijdschrift voor geneeskunde 2007;151(15):863-7.
2007: Cora M Aalfs; Ellen M A Smets; Nico J Leschot
Genetic counselling for familial conditions during pregnancy: a review of the literature published during the years 1989-2004.
Community genetics 2007;10(3):159-68.
2006: G Henrike Westerveld; Cindy M Korver; A M M van Pelt; Nico J Leschot; Fulco van der Veen; Sjoerd Repping; M Paola Lombardi
Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure.
Human reproduction (Oxford, England) 2006;21(12):3178-84.
2006: E M A Boormans; jan van lith; Caterina M Bilardo; Alida C Knegt; D Oepkes; M J V Hoffer; E M J Boon; Hajo I J Wildschut; R J H Galjaard; G Heleen Schuring-Blom; A C C van Oppen; Arie P T Smits; J Creemers; A Go; A Nieuwint; Jan G Nijhuis; C de Die; Gouke J Bonsel; E Birnie; Nico J Leschot
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].
Nederlands tijdschrift voor geneeskunde 2006;150(44):2455; author reply 2455.
2006: M C B van Zwieten; Nico J Leschot; D L Willems
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].
Nederlands tijdschrift voor geneeskunde 2006;150(44):2454; author reply 2454.
2006: Nico J Leschot
['Multifactorial disorders in the genomics era'; notes on a recent report from The Royal Netherlands Academy of Arts and Sciences].
Nederlands tijdschrift voor geneeskunde 2006;150(43):2350-2.
2006: Myra C B van Zwieten; Dick L Willems; Lia Knegt; Nico J Leschot
Communication with patients during the prenatal testing procedure: an explorative qualitative study.
Patient education and counseling 2006;63(1-2):161-8.
2006: M T M Franssen; Johanna C Korevaar; Fulco van der Veen; Nico J Leschot; Patrick Bossuyt; Mariette Goddijn
Reproductive outcome after chromosome analysis in couples with two or more miscarriages: index [corrected]-control study.
BMJ (Clinical research ed.) 2006;332(7544):759-63.
2006: Cora M Aalfs; Frans J Oort; Hanneke C J M de Haes; Nico J Leschot; Ellen M A Smets
Counselor-counselee interaction in reproductive genetic counseling: Does a pregnancy in the counselee make a difference?
Patient education and counseling 2006;60(1):80-90.
2005: M T M Franssen; Johanna C Korevaar; Nico J Leschot; Patrick Bossuyt; Alida C Knegt; Klasien B J Gerssen-Schoorl; Cokkie H Wouters; K B M Hansson; Ron Hochstenbach; Kamlesh Madan; Fulco van der Veen; Mariette Goddijn
Selective chromosome analysis in couples with two or more miscarriages: case-control study.
BMJ (Clinical research ed.) 2005;331(7509):137-41.
2005: Myra C B van Zwieten; Dick L Willems; Liesbeth L Litjens; Heleen G Schuring-Blom; Nico J Leschot
How unexpected are unexpected findings in prenatal cytogenetic diagnosis? A literature review.
European journal of obstetrics, gynecology, and reproductive biology 2005;120(1):15-21.
2005: G Henrike Westerveld; Sjoerd Repping; Nico J Leschot; Fulco van der Veen; M Paola Lombardi
Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis.
Fertility and sterility 2005;83(2):513-5.
2005: S Kapma; Nico J Leschot; Cora M Aalfs
[DNA-analysis in hereditary cancer: the importance of a reliable family history].
Nederlands tijdschrift voor geneeskunde 2005;149(2):57-60.
2005: Mariette Goddijn; Marja van Stralen; Heleen Schuring-Blom; Bert Redeker; Liesbeth van Leeuwen; Sjoerd Repping; Nico J Leschot; Fulco van der Veen
Detection of chromosome abnormalities by quantitative fluorescent PCR in ectopic pregnancies.
Gynecologic and obstetric investigation 2005;60(3):139-44.
2004: Nico J Leschot; marcel mannens
[The disquieting consequences of granting patents on human genes for healthcare and scientific research in The Netherlands].
Nederlands tijdschrift voor geneeskunde 2004;148(35):1712-5.
2004: Cora M Aalfs; ED Mollema; Frans J Oort; J C J M de Haes; Nico J Leschot; Ellen M A Smets
Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics.
Clinical genetics 2004;66(2):112-21.
2004: H T C Nagel; Alida C Knegt; M D Kloosterman; Hajo I J Wildschut; Nico J Leschot; F P H A Vandenbussche
[Invasive prenatal diagnosis in the Netherlands, 1991-2000: number of procedures, indications and abnormal results detected].
Nederlands tijdschrift voor geneeskunde 2004;148(31):1538-43.
2004: G Henrike Westerveld; Judith Gianotten; Nico J Leschot; Fulco van der Veen; Sjoerd Repping; M Paola Lombardi
Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesis.
Molecular human reproduction 2004;10(4):265-9.
2004: Mariette Goddijn; J H K Joosten; Alida C Knegt; F van derVeen; M T M Franssen; Gouke J Bonsel; Nico J Leschot
Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage.
Human reproduction (Oxford, England) 2004;19(4):1013-7.
2004: Judith Gianotten; G Henrike Westerveld; Nico J Leschot; Michael W T Tanck; Richard Lilford; M Paola Lombardi; Fulco van der Veen
Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern.
Human reproduction (Oxford, England) 2004;19(1):71-6.
2003: Judith Gianotten; Fulco van der Veen; Marielle Alders; Nico J Leschot; Michael W T Tanck; Jolande A Land; Jan A M Kremer; Lies Hoefsloot; marcel mannens; M Paola Lombardi; Mariëtte J V Hoffer
Chromosomal region 11p15 is associated with male factor subfertility.
Molecular human reproduction 2003;9(10):587-92.
2003: Judith Gianotten; Mariëtte J V Hoffer; Jan W A de Vries; Nico J Leschot; Jan Gerris; Fulco van der Veen
Partial DAZ deletions in a family with five infertile brothers.
Fertility and sterility 2003;79 Suppl 3():1652-5.
2003: Sjoerd Repping; Jan W A de Vries; Saskia K M van Daalen; Cindy M Korver; Nico J Leschot; Fulco van der Veen
The use of spermHALO-FISH to determine DAZ gene copy number.
Molecular human reproduction 2003;9(4):183-8.
2003: Cora M Aalfs; Ellen M A Smets; Hanneke C J M de Haes; Nico J Leschot
Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs.
Family practice 2003;20(2):135-41.
2003: Irene M van Langen; Erwin Birnie; Nico J Leschot; Gouke J Bonsel; Arthur A M Wilde
Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?
European heart journal 2003;24(6):560-6.
2002: Jan W A de Vries; Sjoerd Repping; Saskia K M van Daalen; Cindy M Korver; Nico J Leschot; Fulco van der Veen
Clinical relevance of partial AZFc deletions.
Fertility and sterility 2002;78(6):1209-14.
2002: Arty H P Schaap; Hans G van der Pol; Kees Boer; Nico J Leschot; Hans Wolf
Long-term follow-up of infants after transcervical chorionic villus sampling and after amniocentesis to compare congenital abnormalities and health status.
Prenatal diagnosis 2002;22(7):598-604.
2002: G Heleen Schuring-Blom; Kees Boer; Alida C Knegt; Marjan Verjaal; Nico J Leschot
Trisomy 13 or 18 (mosaicism) in first trimester cytotrophoblast cells: false-positive results in 11 out of 51 cases.
European journal of obstetrics, gynecology, and reproductive biology 2002;101(2):161-8.
2002: Jan W A de Vries; Mariëtte J V Hoffer; Sjoerd Repping; Jan M N Hoovers; Nico J Leschot; Fulco van der Veen
Reduced copy number of DAZ genes in subfertile and infertile men.
Fertility and sterility 2002;77(1):68-75.
2001: G Heleen Schuring-Blom; Jan M N Hoovers; jan van lith; Alida C Knegt; Nico J Leschot
FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy.
Prenatal diagnosis 2001;21(10):864-7.
2001: Cora M Aalfs; E M Smets; J C de Haes; Nico J Leschot
[Prenatal genetic counseling in pregnancy: the importance of (early) timely referral ].
Nederlands tijdschrift voor geneeskunde 2001;145(33):1577-81.
2001: Nico J Leschot
[Use of genetics in the Dutch health care system; a memorandum from the Dutch Minister of Health, Welfare and Sports to the Dutch Parliament].
Nederlands tijdschrift voor geneeskunde 2001;145(26):1233-5.
2001: G Heleen Schuring-Blom; Kees Boer; Nico J Leschot
A placental diploid cell line is not essential for ongoing trisomy 13 or 18 pregnancies.
European journal of human genetics : EJHG 2001;9(4):286-90.
2001: Jan W A de Vries; Sjoerd Repping; Robert D Oates; R Carson; Nico J Leschot; Fulco van der Veen
Absence of deleted in azoospermia (DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions.
Fertility and sterility 2001;75(3):476-9.
2000: Edo M Hoogerwaard; HB Ginjaar; Arthur A M Wilde; Nico J Leschot; Willem G de Voogt; Marianne De Visser
[The heartache of muscular dystrophy].
Nederlands tijdschrift voor geneeskunde 2000;144(46):2181-4.
2000: Mariette Goddijn; Nico J Leschot
Genetic aspects of miscarriage.
Baillière's best practice & research. Clinical obstetrics & gynaecology 2000;14(5):855-65.
2000: Nico J Leschot; marcel mannens
[Decoding of the human genome: a milestone, but not the end of the road].
Nederlands tijdschrift voor geneeskunde 2000;144(23):1093-6.
2000: Joke de Pater; G Heleen Schuring-Blom; M A Nieste-Otter; B van Nesselrooij; B Kapitein; G C M L Christiaens; Nico J Leschot
Trisomy 8 in chorionic villi-unpredictable results in follow-up.
Prenatal diagnosis 2000;20(5):435-7.
2000: Irene M de Graaf; Howard Cuckle; E Pajkrt; Nico J Leschot; Otto P Bleker; jan van lith
Co-variables in first trimester maternal serum screening.
Prenatal diagnosis 2000;20(3):186-9.
1999: Jan M N Hoovers; C H Mellink; Nico J Leschot
[Fluorescence in situ hybridization in the study of chromosomal abnormalities].
Nederlands tijdschrift voor geneeskunde 1999;143(45):2265-8.
1999: M F Mohrschladt; EK Bijlsma; Sigrid Sluijter; R F De Coo; Jan M N Hoovers; Nico J Leschot
A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).
Clinical dysmorphology 1999;8(3):211-4.
1999: Irene M de Graaf; ME Jakobs; Nico J Leschot; Ilya Ravkin; Simon Goldbard; Jan M N Hoovers
Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system.
Prenatal diagnosis 1999;19(7):648-52.
1999: Edo M Hoogerwaard; Pol A van der Wouw; Arthur A M Wilde; Egbert Bakker; P F Ippel; Jan C Oosterwijk; D F Majoor-Krakauer; Anthonie J van Essen; Nico J Leschot; Marianne De Visser
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy.
Neuromuscular disorders : NMD 1999;9(5):347-51.
1999: Edo M Hoogerwaard; Egbert Bakker; P F Ippel; Jan C Oosterwijk; D F Majoor-Krakauer; Nico J Leschot; Anthonie J van Essen; H G Brunner; Pol A van der Wouw; Arthur A M Wilde; Marianne De Visser
Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study.
Lancet 1999;353(9170):2116-9.
1999: Irene M de Graaf; E Pajkrt; Caterina M Bilardo; Nico J Leschot; Howard Cuckle; jan van lith
Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency.
Prenatal diagnosis 1999;19(5):458-62.
1999: Mariette Goddijn; Fulco van der Veen; Willem M Ankum; Gouke J Bonsel; Nico J Leschot; kees boer
[No consensus on the definition, diagnosis and treatment of habitual abortion in the Netherlands].
Nederlands tijdschrift voor geneeskunde 1999;143(17):897-902.
1999: Irene M de Graaf; E Pajkrt; M Keessen; Nico J Leschot; Caterina M Bilardo
Enlarged nuchal translucency and low serum protein concentrations as possible markers for Zellweger syndrome.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 1999;13(4):268-70.
1999: Irene M de Graaf; S M van Bezouw; ME Jakobs; Nico J Leschot; HA Zondervan; Caterina M Bilardo; Jan M N Hoovers
First-trimester non-invasive prenatal diagnosis of triploidy.
Prenatal diagnosis 1999;19(2):175-7.
1998: K Hansson; W M Poelma; HA Zondervan; Nico J Leschot
Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues.
Prenatal diagnosis 1998;18(9):975-8.
1998: Anneke J van der Kooi; Marianne De Visser; MT van Meegen; HB Ginjaar; Anthonie J van Essen; F G I Jennekens; PJ Jongen; Nico J Leschot; PA Bolhuis
A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy.
Neuromuscular disorders : NMD 1998;8(5):305-8.
1997: Irene M van Langen; Cora M Aalfs; E M Smets; J C de Haes; M C Jansweijer; Nico J Leschot
[Genetic counseling: should side issues become main issues?].
Nederlands tijdschrift voor geneeskunde 1997;141(38):1801-4.
1997: Nico J Leschot; M D Kloosterman
Prenatal diagnosis in the Netherlands. Dutch Working Party of Prenatal Diagnosis.
European journal of human genetics : EJHG 1997;5 Suppl 1():51-6.
1997: Joke de Pater; G Heleen Schuring-Blom; R van den Bogaard; C J M van der Sijs-Bos; G C M L Christiaens; Philip Stoutenbeek; Nico J Leschot
Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22.
Prenatal diagnosis 1997;17(1):81-6.
1996: Nico J Leschot
Specific approaches to fetal cells isolation from maternal blood: introduction.
Early human development 1996;47 Suppl():S69-72.
1996: M Goddijn; Fulco van der Veen; G H Schuring-Blom; Willem M Ankum; Nico J Leschot
Cytogenetic characteristics of ectopic pregnancy.
Human reproduction (Oxford, England) 1996;11(12):2769-71.
1996: Nico J Leschot; G H Schuring-Blom; A C Van Prooijen-Knegt; M Verjaal; K Hansson; Hans Wolf; H H Kanhai; J M Van Vugt; G C M L Christiaens
The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells.
Prenatal diagnosis 1996;16(8):705-12.
1996: Irene van Langen; M A Otter; Daniel C Aronson; W C Overweg-Plandsoen; Raoul Hennekam; Nico J Leschot; Jan M N Hoovers
Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.
Clinical genetics 1996;49(1):49-53.
1995: Celia Delozier-Blanchet; L Francipane; Michael Morris; Jan M N Hoovers; Nico J Leschot; J N Cox
Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counseling.
Clinical genetics 1995;48(6):308-12.
1995: Cora M Aalfs; Jan M N Hoovers; M A Nieste-Otter; marcel mannens; Raoul Hennekam; Nico J Leschot
Further delineation of the partial proximal trisomy 10q syndrome.
Journal of medical genetics 1995;32(12):968-71.
1995: K Hansson; G H Schuring-Blom; Nico J Leschot
The preserving of chorionic villi before establishing long-term cell cultures for cytogenetic analysis.
Prenatal diagnosis 1995;15(11):1067-9.
1995: S Lunshof; Kees Boer; Nico J Leschot; M Pomp; Hans Wolf
Pregnancy outcome after transcervical CVS with a flexible biopsy forceps: evaluation of risk factors.
Prenatal diagnosis 1995;15(9):809-16.
1995: Irene van Langen; Nico J Leschot
[Does the (imminent) miscarriage standard of the Dutch College of Family Physicians correspond to its management by gynecologists].
Nederlands tijdschrift voor geneeskunde 1995;139(27):1403; author reply 1404.
1993: G H Schuring-Blom; M Keijzer; M E Jakobs; D M Van den Brande; H M Visser; Joop Wiegant; Jan M N Hoovers; Nico J Leschot
Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization.
Prenatal diagnosis 1993;13(8):671-9.
1993: Jan M N Hoovers; E Redeker; Frank Speleman; J W Höppener; S Bhola; Jet Bliek; Nadine Van Roy; Nico J Leschot; Andries Westerveld; marcel mannens
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.
Genomics 1993;15(3):525-9.
1992: Nico J Leschot; M Verjaal; P E Treffers; M E Richard-Mulder
[Social support following induced abortion for genetic indications: experiences of the women concerned and their partners].
Nederlands tijdschrift voor geneeskunde 1992;136(18):892-3.
1992: Jan M N Hoovers; marcel mannens; R John; Jet Bliek; Veronica van Heyningen; D J Porteous; Nico J Leschot; Andries Westerveld; PF Little
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.
Genomics 1992;12(2):254-63.
1992: J G van der Pol; Hans Wolf; Kees Boer; Pieter E Treffers; Nico J Leschot; H A Hey; A Vos
Jejunal atresia related to the use of methylene blue in genetic amniocentesis in twins.
British journal of obstetrics and gynaecology 1992;99(2):141-3.
1991: Nico J Leschot; Hans Wolf
Is placental mosaicism associated with poor perinatal outcome?
Prenatal diagnosis 1991;11(6):403-4.
1990: Nico J Leschot; H H Kanhai; CJ van Asperen; Hans Wolf; Kees Boer; A C van Prooijen-Knegt; G C M L Christiaens; M Verjaal; E Briet
An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS.
Clinical genetics 1990;38(3):211-7.
1990: Nico J Leschot; Hans Wolf; M Verjaal; A C van Prooijen-Knegt; Kees Boer
Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma.
Clinical genetics 1990;37(3):236-7.
1990: H Wolf; Nico J Leschot; M T van den Kroonenberg; N Walford; F B Lammes
[Prenatal diagnosis of triploidy].
Nederlands tijdschrift voor geneeskunde 1990;134(8):394-7.
1989: Nico J Leschot; Hans Wolf; A C Van Prooijen-Knegt; CJ van Asperen; M Verjaal; G H Schuring-Blom; Kees Boer; H H Kanhai; G C M L Christiaens
Cytogenetic findings in 1250 chorionic villus samples obtained in the first trimester with clinical follow-up of the first 1000 pregnancies.
British journal of obstetrics and gynaecology 1989;96(6):663-70.
1989: G C M L Christiaens; J Van Baarlen; J Huber; Nico J Leschot
Fetal limb constriction: a possible complication of CVS.
Prenatal diagnosis 1989;9(1):67-71.
1988: Nico J Leschot; Hans Wolf; G H Weenink
False negative findings at third trimester chorionic villus sampling (C.V.S.).
Clinical genetics 1988;34(3):204-5.
1988: Nico J Leschot; E J Wilmsen-Linders; H P van Geijn; J F Samsom; L M Smit
Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesis.
Clinical genetics 1988;34(2):135-9.
1988: T J Herweijer; J W Oorthuys; Nico J Leschot
De novo partial trisomy 15q (proximal type).
Journal of medical genetics 1988;25(4):260-2.
1988: Anthony de Ronde; marcel mannens; R M Slater; Jan M N Hoovers; Christa Heyting; EM Bleeker-Wagemakers; Nico J Leschot; A van Strien; Cees Sol; Jan ter Schegget
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11.
The Journal of general virology 1988;69 ( Pt 2)():467-71.
1987: Nico J Leschot; Hans Wolf; M Verjaal; L C van Prooijen-Knegt; E G de Boer; H H Kanhai; G C M L Christiaens
Chorionic villi sampling: cytogenetic and clinical findings in 500 pregnancies.
British medical journal (Clinical research ed.) 1987;295(6595):407-10.
1987: M Verjaal; Nico J Leschot; H Wolf; P E Treffers
Karyotypic differences between cells from placenta and other fetal tissues.
Prenatal diagnosis 1987;7(5):343-8.
1985: Nico J Leschot; M Verjaal; P E Treffers
Risks of midtrimester amniocentesis; assessment in 3000 pregnancies.
British journal of obstetrics and gynaecology 1985;92(8):804-7.
1985: Nico J Leschot; M Verjaal; P E Treffers
Therapeutic abortion following midtrimester amniocentesis.
Prenatal diagnosis 1985;5(3):243-4.
1985: Nico J Leschot; Christa Heyting; M V Schaik; E J Redeker
Amniotic fluid gel acetylcholinesterase determination in prenatal diagnosis: dark field illumination as a method for improving the detection of precipitation bands.
Prenatal diagnosis 1985;5(3):237-41.
1985: Nico J Leschot; M Verjaal; P E Treffers
A critical analysis of 75 therapeutic abortions.
Early human development 1985;10(3-4):287-93.
1982: M Verjaal; Nico J Leschot; P E Treffers
Women's experiences with second trimester prenatal diagnosis.
Prenatal diagnosis 1982;2(3):195-209.
1981: M Verjaal; Nico J Leschot; P E Treffers
Risk of amniocentesis and laboratory findings in a series of 1500 prenatal diagnoses.
Prenatal diagnosis 1981;1(3):173-81.
1981: P E Treffers; Nico J Leschot; M Verjaal
[Amniotic fluid analysis in the 2d pregnancy trimester].
Nederlands tijdschrift voor geneeskunde 1981;125(13):489-93.
1980: Nico J Leschot; P E Treffers; M J Becker-Bloemkolk; S van Zanten; W P de Groot; M Verjaal
Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parameters.
European journal of obstetrics, gynecology, and reproductive biology 1980;10(6):381-8.
1980: M Verjaal; A H Meyer; M J Becker-Bloemkolk; Nico J Leschot; J J der Weduwen; J G Gras
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome.
American journal of medical genetics 1980;7(1):85-6.