Username

Password

Forgot Password?

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Nico Leschot

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Physiology

Procedures

Disorders

Occupations

Genetic Counseling

Geographic Areas

Netherlands

Living Beings

Newborn Infant

Concepts & Ideas

Anatomy

X Chromosome

Sign-in to see full Profile

Network (preview)

Co-Publications
Name
18
van der Veen, Fulco
13
Hoovers, Jan
10
Wolf, Hans
9
Goddijn, Mariette
9
Aalfs, Cora
8
Boer, Kees
8
Knegt, Alida
8
Repping, Sjoerd
7
Christiaens, G C M L
7
mannens, marcel
6
Franssen, M T M
6
Schuring-Blom, Heleen
6
Smets, Ellen
5
Korevaar, Johanna
5
Lombardi, Paola

Sign-in to see all Coauthors

Publications

TOP 3
Mollema E D; Smets E M A; Richard M E; Schiphorst A M; Leschot N J
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.
Franssen M T M; Korevaar J C; Tjoa W M; Leschot N J; Bossuyt P M M; Knegt A C; Suykerbuyk R F; Hochstenbach R; van der Veen F; Goddijn M
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.
Aalfs C M; Oort F J; de Haes J C J M; Leschot N J; Smets E M A
A comparison of counselee and counselor satisfaction in reproductive genetic counseling.

Sign-in to see all Publications

Sign in free and see...

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 visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Nico Leschot (preview)

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

Flash Player Required

Sign-in to see more

All Publications

2008: Mollema E D; Smets E M A; Richard M E; Schiphorst A M; Leschot N J
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: Franssen M T M; Korevaar J C; Tjoa W M; Leschot N J; Bossuyt P M M; Knegt A C; Suykerbuyk R F; Hochstenbach R; van der Veen F; Goddijn M
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.
Prenatal diagnosis 2008;28(5):408-11.
2007: Aalfs C M; Oort F J; de Haes J C J M; Leschot N J; Smets E M A
A comparison of counselee and counselor satisfaction in reproductive genetic counseling.
Clinical genetics 2007;72(2):74-82.
2007: Leschot N J; Wilde A A M
[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: Franssen M T M; Korevaar J C; van der Veen F; Boer K; Leschot N J; Goddijn M
Management of recurrent miscarriage: evaluating the impact of a guideline.
Human reproduction (Oxford, England) 2007;22(5):1298-303.
2007: Franssen M T M; Korevaar J C; Leschot N J; Bossuyt P M M; Knegt A C; Gerssen-Schoorl K B J; Wouters C H; Hansson K B M; Hochstenbach P F R; Madan K; van der Veen F; Goddijn M
[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: Aalfs C M; Smets E M A; Leschot N J
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: Westerveld G H; Korver C M; van Pelt A M M; Leschot N J; van der Veen F; Repping S; Lombardi M P
Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure.
Human reproduction (Oxford, England) 2006;21(12):3178-84.
2006: Boormans E M A; van Lith J M M; Bilardo C M; Knegt A C; Oepkes D; Hoffer M J V; Boon E M J; Wildschut H I J; Galjaard R J H; Schuring-Blom G H; van Oppen A C C; Smits A; Creemers J; Go A; Nieuwint A; Nijhuis J G; de Die C; Bonsel G J; Birnie E; Leschot N
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities]
Nederlands tijdschrift voor geneeskunde 2006;150(44):2455; author reply 2455.
2006: van Zwieten M C B; Leschot N J; Willems D L
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities]
Nederlands tijdschrift voor geneeskunde 2006;150(44):2454; author reply 2454.
2006: Leschot N J
['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: van Zwieten Myra; Willems Dick; Knegt Lia; Leschot Nico
Communication with patients during the prenatal testing procedure: an explorative qualitative study.
Patient education and counseling 2006;63(1-2):161-8.
2006: Franssen Maureen T M; Korevaar Johanna C; van der Veen Fulco; Leschot Nico J; Bossuyt Patrick M M; Goddijn Mariette
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: Aalfs Cora M; Oort Frans J; de Haes Hanneke C J M; Leschot Nico J; Smets Ellen M A
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: Franssen Maureen T M; Korevaar Johanna C; Leschot Nico J; Bossuyt Patrick M M; Knegt Alida C; Gerssen-Schoorl Klasien B J; Wouters Cokkie H; Hansson Kerstin B M; Hochstenbach Ron; Madan Kamlesh; van der Veen Fulco; Goddijn Mariette
Selective chromosome analysis in couples with two or more miscarriages: case-control study.
BMJ (Clinical research ed.) 2005;331(7509):137-41.
2005: van Zwieten Myra C B; Willems Dick L; Litjens Liesbeth L; Schuring-Blom Heleen G; Leschot Nico
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: Westerveld G Henrike; Repping Sjoerd; Leschot Nico J; van der Veen Fulco; Lombardi M Paola
Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis.
Fertility and sterility 2005;83(2):513-5.
2005: Kapma S; Leschot N J; Aalfs C M
[DNA-analysis in hereditary cancer: the importance of a reliable family history]
Nederlands tijdschrift voor geneeskunde 2005;149(2):57-60.
2005: Goddijn Mariette; van Stralen Marja; Schuring-Blom Heleen; Redeker Bert; van Leeuwen Liesbeth; Repping Sjoerd; Leschot Nico; van der Veen Fulco
Detection of chromosome abnormalities by quantitative fluorescent PCR in ectopic pregnancies.
Gynecologic and obstetric investigation 2005;60(3):139-44.
2004: Leschot N J; Mannens M M A M
[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: Aalfs C M; Mollema E D; Oort F J; de Haes J C J M; Leschot N J; Smets E M A
Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics.
Clinical genetics 2004;66(2):112-21.
2004: Nagel H T C; Knegt A C; Kloosterman M D; Wildschut H I J; Leschot N J; Vandenbussche F P H A
[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: Westerveld G H; Gianotten J; Leschot N J; van der Veen F; Repping S; Lombardi M P
Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesis.
Molecular human reproduction 2004;10(4):265-9.
2004: Goddijn M; Joosten J H K; Knegt A C; van derVeen F; Franssen M T M; Bonsel G J; Leschot N J
Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage.
Human reproduction (Oxford, England) 2004;19(4):1013-7.
2004: Gianotten Judith; Westerveld G Henrike; Leschot Nico J; Tanck Michael W T; Lilford Richard J; Lombardi M Paola; van der Veen Fulco
Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern.
Human reproduction (Oxford, England) 2004;19(1):71-6.
2003: Gianotten Judith; van der Veen Fulco; Alders Mariëlle; Leschot Nico J; Tanck Michael W T; Land Jolande A; Kremer Jan A M; Hoefsloot Lies H; Mannens Marcel M; Lombardi M Paola; Hoffer Mariëtte J V
Chromosomal region 11p15 is associated with male factor subfertility.
Molecular human reproduction 2003;9(10):587-92.
2003: Gianotten Judith; Hoffer Mariëtte J V; De Vries Jan W A; Leschot Nico J; Gerris Jan; van der Veen Fulco
Partial DAZ deletions in a family with five infertile brothers.
Fertility and sterility 2003;79 Suppl 3():1652-5.
2003: Repping Sjoerd; de Vries Jan W A; van Daalen Saskia K M; Korver Cindy M; Leschot Nico J; van der Veen Fulco
The use of spermHALO-FISH to determine DAZ gene copy number.
Molecular human reproduction 2003;9(4):183-8.
2003: Aalfs Cora M; Smets Ellen M A; de Haes Hanneke C J M; Leschot Nico J
Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs.
Family practice 2003;20(2):135-41.
2003: van Langen I M; Birnie E; Leschot N J; Bonsel G J; Wilde A A M
Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?
European heart journal 2003;24(6):560-6.
2002: de Vries Jan W A; Repping Sjoerd; van Daalen Saskia K M; Korver Cindy M; Leschot Nico J; van der Veen Fulco
Clinical relevance of partial AZFc deletions.
Fertility and sterility 2002;78(6):1209-14.
2002: Schaap Arty H P; van der Pol Hans G; Boer Kees; Leschot Nico J; Wolf Hans
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: Schuring-Blom G Heleen; Boer Kees; Knegt Alida C; Verjaal Marjan; Leschot Nico J
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: de Vries Jan W A; Hoffer Mariëtte J V; Repping Sjoerd; Hoovers Jan M N; Leschot Nico J; van der Veen Fulco
Reduced copy number of DAZ genes in subfertile and infertile men.
Fertility and sterility 2002;77(1):68-75.
2001: Schuring-Blom G H; Hoovers J M; van Lith J M; Knegt A C; Leschot N J
FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy.
Prenatal diagnosis 2001;21(10):864-7.
2001: Aalfs C M; Smets E M; de Haes J C; Leschot N J
[Prenatal genetic counseling in pregnancy: the importance of (early) timely referral ]
Nederlands tijdschrift voor geneeskunde 2001;145(33):1577-81.
2001: Leschot N J
[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: Schuring-Blom G H; Boer K; Leschot N J
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: de Vries J W; Repping S; Oates R; Carson R; Leschot N J; van der Veen F
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: Hoogerwaard E M; Ginjaar H B; Wilde A A; Leschot N J; de Voogt W G; de Visser M
[The heartache of muscular dystrophy]
Nederlands tijdschrift voor geneeskunde 2000;144(46):2181-4.
2000: Goddijn M; Leschot N J
Genetic aspects of miscarriage.
Baillière's best practice & research. Clinical obstetrics & gynaecology 2000;14(5):855-65.
2000: Leschot N J; Mannens M M
[Decoding of the human genome: a milestone, but not the end of the road]
Nederlands tijdschrift voor geneeskunde 2000;144(23):1093-6.
2000: de Pater J M; Schuring-Blom G H; Nieste-Otter M A; van Nesselrooij B; Kapitein B; Christiaens G C; Leschot N J
Trisomy 8 in chorionic villi-unpredictable results in follow-up.
Prenatal diagnosis 2000;20(5):435-7.
2000: de Graaf I M; Cuckle H S; Pajkrt E; Leschot N J; Bleker O P; van Lith J M
Co-variables in first trimester maternal serum screening.
Prenatal diagnosis 2000;20(3):186-9.
1999: Hoovers J M; Mellink C H; Leschot N J
[Fluorescence in situ hybridization in the study of chromosomal abnormalities]
Nederlands tijdschrift voor geneeskunde 1999;143(45):2265-8.
1999: Mohrschladt M F; Bijlsma E K; Sluijter S; De Coo R F; Hoovers J M; Leschot N J
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: de Graaf I M; Jakobs M E; Leschot N J; Ravkin I; Goldbard S; Hoovers J M
Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system.
Prenatal diagnosis 1999;19(7):648-52.
1999: Hoogerwaard E M; van der Wouw P A; Wilde A A; Bakker E; Ippel P F; Oosterwijk J C; Majoor-Krakauer D F; van Essen A J; Leschot N J; de Visser M
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy.
Neuromuscular disorders : NMD 1999;9(5):347-51.
1999: Hoogerwaard E M; Bakker E; Ippel P F; Oosterwijk J C; Majoor-Krakauer D F; Leschot N J; Van Essen A J; Brunner H G; van der Wouw P A; Wilde A A; de Visser M
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: de Graaf I M; Pajkrt E; Bilardo C M; Leschot N J; Cuckle H S; van Lith J M
Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency.
Prenatal diagnosis 1999;19(5):458-62.
1999: Goddijn M; van der Veen F; Ankum W M; Bonsel G J; Leschot N J; Boer K
[No consensus on the definition, diagnosis and treatment of habitual abortion in the Netherlands]
Nederlands tijdschrift voor geneeskunde 1999;143(17):897-902.
1999: de Graaf I M; Pajkrt E; Keessen M; Leschot N J; Bilardo C M
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: de Graaf I M; van Bezouw S M; Jakobs M E; Leschot N J; Zondervan H A; Bilardo C M; Hoovers J M
First-trimester non-invasive prenatal diagnosis of triploidy.
Prenatal diagnosis 1999;19(2):175-7.
1998: Hansson K; Poelma W M; Zondervan H A; Leschot N J
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: van der Kooi A J; de Visser M; van Meegen M; Ginjaar H B; van Essen A J; Jennekens F G; Jongen P J; Leschot N J; Bolhuis P A
A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy.
Neuromuscular disorders : NMD 1998;8(5):305-8.
1997: van Langen I M; Aalfs C M; Smets E M; de Haes J C; Jansweijer M C; Leschot N J
[Genetic counseling: should side issues become main issues?]
Nederlands tijdschrift voor geneeskunde 1997;141(38):1801-4.
1997: de Pater J M; Schuring-Blom G H; van den Bogaard R; van der Sijs-Bos C J; Christiaens G C; Stoutenbeek P; Leschot N J
Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22.
Prenatal diagnosis 1997;17(1):81-6.
1997: Leschot N J; Kloosterman M D
Prenatal diagnosis in the Netherlands. Dutch Working Party of Prenatal Diagnosis.
European journal of human genetics : EJHG 1997;5 Suppl 1():51-6.
1996: Leschot N J
Specific approaches to fetal cells isolation from maternal blood: introduction.
Early human development 1996;47 Suppl():S69-72.
1996: Goddijn M; van der Veen F; Schuring-Blom G H; Ankum W M; Leschot N J
Cytogenetic characteristics of ectopic pregnancy.
Human reproduction (Oxford, England) 1996;11(12):2769-71.
1996: Leschot N J; Schuring-Blom G H; Van Prooijen-Knegt A C; Verjaal M; Hansson K; Wolf H; Kanhai H H; Van Vugt J M; Christiaens G C
The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells.
Prenatal diagnosis 1996;16(8):705-12.
1996: van Langen I M; Otter M A; Aronson D C; Overweg-Plandsoen W C; Hennekam R C; Leschot N J; Hoovers J M
Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.
Clinical genetics 1996;49(1):49-53.
1995: Delozier-Blanchet C D; Francipane L; Morris M A; Hoovers J M; Leschot N J; Cox J N
Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counseling.
Clinical genetics 1995;48(6):308-12.
1995: Aalfs C M; Hoovers J M; Nieste-Otter M A; Mannens M M; Hennekam R C; Leschot N J
Further delineation of the partial proximal trisomy 10q syndrome.
Journal of medical genetics 1995;32(12):968-71.
1995: Hansson K; Schuring-Blom G H; Leschot N J
The preserving of chorionic villi before establishing long-term cell cultures for cytogenetic analysis.
Prenatal diagnosis 1995;15(11):1067-9.
1995: Lunshof S; Boer K; Leschot N J; Pomp M; Wolf H
Pregnancy outcome after transcervical CVS with a flexible biopsy forceps: evaluation of risk factors.
Prenatal diagnosis 1995;15(9):809-16.
1995: van Langen I M; Leschot N J
[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: Schuring-Blom G H; Keijzer M; Jakobs M E; Van den Brande D M; Visser H M; Wiegant J; Hoovers J M; Leschot N J
Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization.
Prenatal diagnosis 1993;13(8):671-9.
1993: Hoovers J M; Redeker E; Speleman F; Höppener J W; Bhola S; Bliek J; van Roy N; Leschot N J; Westerveld A; Mannens M
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.
Genomics 1993;15(3):525-9.
1992: Leschot N J; Verjaal M; Treffers P E; Richard-Mulder M E
[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: Hoovers J M; Mannens M; John R; Bliek J; van Heyningen V; Porteous D J; Leschot N J; Westerveld A; Little P F
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.
Genomics 1992;12(2):254-63.
1992: van der Pol J G; Wolf H; Boer K; Treffers P E; Leschot N J; Hey H A; Vos A
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: Leschot N J; Wolf H
Is placental mosaicism associated with poor perinatal outcome?
Prenatal diagnosis 1991;11(6):403-4.
1990: Leschot N J; Kanhai H H; van Asperen C J; Wolf H; Boer K; van Prooijen-Knegt A C; Christiaens G C; Verjaal M; Briet E
An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS.
Clinical genetics 1990;38(3):211-7.
1990: Leschot N J; Wolf H; Verjaal M; van Prooijen-Knegt A C; Boer K
Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma.
Clinical genetics 1990;37(3):236-7.
1990: Wolf H; Leschot N J; van den Kroonenberg M T; Walford N; Lammes F B
[Prenatal diagnosis of triploidy]
Nederlands tijdschrift voor geneeskunde 1990;134(8):394-7.
1989: Leschot N J; Wolf H; Van Prooijen-Knegt A C; van Asperen C J; Verjaal M; Schuring-Blom G H; Boer K; Kanhai H H; Christiaens G C
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: Christiaens G C; Van Baarlen J; Huber J; Leschot N J
Fetal limb constriction: a possible complication of CVS.
Prenatal diagnosis 1989;9(1):67-71.
1988: Leschot N J; Wolf H; Weenink G H
False negative findings at third trimester chorionic villus sampling (C.V.S.).
Clinical genetics 1988;34(3):204-5.
1988: Leschot N J; Wilmsen-Linders E J; van Geijn H P; Samsom J F; Smit L M
Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesis.
Clinical genetics 1988;34(2):135-9.
1988: Herweijer T J; Oorthuys J W; Leschot N J
De novo partial trisomy 15q (proximal type).
Journal of medical genetics 1988;25(4):260-2.
1988: de Ronde A; Mannens M; Slater R M; Hoovers J; Heyting C; Bleeker-Wagemakers E M; Leschot N J; van Strien A; Sol C J; ter Schegget J
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: Leschot N J; Wolf H; Verjaal M; van Prooijen-Knegt L C; de Boer E G; Kanhai H H; Christiaens G C
Chorionic villi sampling: cytogenetic and clinical findings in 500 pregnancies.
British medical journal (Clinical research ed.) 1987;295(6595):407-10.
1987: Verjaal M; Leschot N J; Wolf H; Treffers P E
Karyotypic differences between cells from placenta and other fetal tissues.
Prenatal diagnosis 1987;7(5):343-8.
1985: Leschot N J; Verjaal M; Treffers P E
Risks of midtrimester amniocentesis; assessment in 3000 pregnancies.
British journal of obstetrics and gynaecology 1985;92(8):804-7.
1985: Leschot N J; Verjaal M; Treffers P E
Therapeutic abortion following midtrimester amniocentesis.
Prenatal diagnosis 1985;5(3):243-4.
1985: Leschot N J; Heyting C; Schaik M V; Redeker E J
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: Leschot N J; Verjaal M; Treffers P E
A critical analysis of 75 therapeutic abortions.
Early human development 1985;10(3-4):287-93.
1982: Verjaal M; Leschot N J; Treffers P E
Women's experiences with second trimester prenatal diagnosis.
Prenatal diagnosis 1982;2(3):195-209.
1981: Verjaal M; Leschot N J; Treffers P E
Risk of amniocentesis and laboratory findings in a series of 1500 prenatal diagnoses.
Prenatal diagnosis 1981;1(3):173-81.
1981: Treffers P E; Leschot N J; Verjaal M
[Amniotic fluid analysis in the 2d pregnancy trimester]
Nederlands tijdschrift voor geneeskunde 1981;125(13):489-93.
1980: Leschot N J; Treffers P E; Becker-Bloemkolk M J; van Zanten S; de Groot W P; Verjaal M
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: Verjaal M; Meyer A H; Becker-Bloemkolk M J; Leschot N J; der Weduwen J J; Gras J G
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome.
American journal of medical genetics 1980;7(1):85-6.

Sign-in to see more