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Martin Bobrow

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)

Disorders

Anatomy

X Chromosome

Concepts & Ideas

Chemicals & Drugs

Procedures

Physiology

Occupations

Genetic Counseling

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Publications

TOP 3
Marteau Theresa; Senior Victoria; Humphries Steve E; Bobrow Martin; Cranston Treena; Crook Martin A; Day Lorna; Fernandez Maryam; Horne Rob; Iversen Andrew; Jackson Zoe; Lynas Jacqui; Middleton-Price Helen; Savine Richard; Sikorski Jim; Watson Melanie; Weinman John; Wierzbicki Anthony S; Wray Richard;
Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: a randomized controlled trial.
Marteau Theresa M; Nippert Irma; Hall Sue; Limbert Caroline; Reid Margaret; Bobrow Martin; Cameron Alan; Cornel Martina; van Diem Mariet; Eiben Bernd; García-Miñaur Sixto; Goujard Janine; Kirwan Donna; McIntosh Karen; Soothill Peter; Verschuuren-Bemelmans Corien; de Vigan Catherine; Walkinshaw Stephen; Abramsky Lenore; Louwen Frank; Miny Peter; Horst Jürgen;
Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals.
Michie S; Bobrow M; Marteau T M
Predictive genetic testing in children and adults: a study of emotional impact.

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All Publications

2004: Marteau Theresa; Senior Victoria; Humphries Steve E; Bobrow Martin; Cranston Treena; Crook Martin A; Day Lorna; Fernandez Maryam; Horne Rob; Iversen Andrew; Jackson Zoe; Lynas Jacqui; Middleton-Price Helen; Savine Richard; Sikorski Jim; Watson Melanie; Weinman John; Wierzbicki Anthony S; Wray Richard;
Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: a randomized controlled trial.
American journal of medical genetics. Part A 2004;128A(3):285-93.
2002: Marteau Theresa M; Nippert Irma; Hall Sue; Limbert Caroline; Reid Margaret; Bobrow Martin; Cameron Alan; Cornel Martina; van Diem Mariet; Eiben Bernd; García-Miñaur Sixto; Goujard Janine; Kirwan Donna; McIntosh Karen; Soothill Peter; Verschuuren-Bemelmans Corien; de Vigan Catherine; Walkinshaw Stephen; Abramsky Lenore; Louwen Frank; Miny Peter; Horst Jürgen;
Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals.
Prenatal diagnosis 2002;22(7):562-6.
2001: Michie S; Bobrow M; Marteau T M
Predictive genetic testing in children and adults: a study of emotional impact.
Journal of medical genetics 2001;38(8):519-26.
2001: Pembrey M E; Barnicoat A J; Carmichael B; Bobrow M; Turner G
An assessment of screening strategies for fragile X syndrome in the UK.
Health technology assessment (Winchester, England) 2001;5(7):1-95.
2000: Marteau T M; Saidi G; Goodburn S; Lawton J; Michie S; Bobrow M
Numbers or words? A randomized controlled trial of presenting screen negative results to pregnant women.
Prenatal diagnosis 2000;20(9):714-8.
2000: Johnson M R; Ferner R E; Bobrow M; Hughes R A
Detailed analysis of the oligodendrocyte myelin glycoprotein gene in four patients with neurofibromatosis 1 and primary progressive multiple sclerosis.
Journal of neurology, neurosurgery, and psychiatry 2000;68(5):643-6.
2000: Hall S; Bobrow M; Marteau T M
Psychological consequences for parents of false negative results on prenatal screening for Down's syndrome: retrospective interview study.
BMJ (Clinical research ed.) 2000;320(7232):407-12.
1999: Smith T A; Yau S C; Bobrow M; Abbs S J
Identification and quantification of somatic mosaicism for a point mutation in a Duchenne muscular dystrophy family.
Journal of medical genetics 1999;36(4):313-5.
1998: Michie S; Allanson A; Armstrong D; Weinman J; Bobrow M; Marteau T M
Objectives of genetic counselling: differing views of purchasers, providers and users.
Journal of public health medicine 1998;20(4):404-8.
1997: Michie S; French D; Allanson A; Bobrow M; Marteau T M
Information recall in genetic counselling: a pilot study of its assessment.
Patient education and counseling 1997;32(1-2):93-100.
1997: Michie S; Marteau T M; Bobrow M
Genetic counselling: the psychological impact of meeting patients' expectations.
Journal of medical genetics 1997;34(3):237-41.
1997: Barnicoat A J; Wang Q; Turk J; Green E; Mathew C G; Flynn G; Buckle V; Hirst M; Davies K; Bobrow M
Clinical, cytogenetic, and molecular analysis of three families with FRAXE.
Journal of medical genetics 1997;34(1):13-7.
1997: Michie S; Bron F; Bobrow M; Marteau T M
Nondirectiveness in genetic counseling: an empirical study.
American journal of human genetics 1997;60(1):40-7.
1996: Roberts R G; Kendall E; Vetrie D; Bobrow M
Sequence and chromosomal location of a human homologue of LRPR1, an FSH primary response gene.
Genomics 1996;37(1):122-4.
1996: Yau S C; Bobrow M; Mathew C G; Abbs S J
Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.
Journal of medical genetics 1996;33(7):550-8.
1996: Roberts R G; Freeman T C; Kendall E; Vetrie D L; Dixon A K; Shaw-Smith C; Bone Q; Bobrow M
Characterization of DRP2, a novel human dystrophin homologue.
Nature genetics 1996;13(2):223-6.
1996: Axworthy D; Brock D J; Bobrow M; Marteau T M
Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up. UK Cystic Fibrosis Follow-Up Study Group.
Lancet 1996;347(9013):1443-6.
1996: Michie S; McDonald V; Bobrow M; McKeown C; Marteau T
Parents' responses to predictive genetic testing in their children: report of a single case study.
Journal of medical genetics 1996;33(4):313-8.
1995: Marteau T; Michie S; Drake H; Bobrow M
Public attitudes towards the selection of desirable characteristics in children.
Journal of medical genetics 1995;32(10):796-8.
1995: Gardner R J; Bobrow M; Roberts R G
The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test.
American journal of human genetics 1995;57(2):311-20.
1995: Jin H; Webster A D; Vihinen M; Sideras P; Vorechovsky I; Hammarstróm L; Bernatowska-Matuszkiewicz E; Smith C I; Bobrow M; Vetrie D
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA).
Human molecular genetics 1995;4(4):693-700.
1995: Wang Q; Green E; Bobrow M; Mathew C G
A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci.
Journal of medical genetics 1995;32(3):170-3.
1995: Boye E; Flinter F; Zhou J; Tryggvason K; Bobrow M; Harris A
Detection of 12 novel mutations in the collagenous domain of the COL4A5 gene in Alport syndrome patients.
Human mutation 1995;5(3):197-204.
1994: Ritchie R J; Knight S J; Hirst M C; Grewal P K; Bobrow M; Cross G S; Davies K E
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
Human molecular genetics 1994;3(12):2115-21.
1994: Marteau T; Drake H; Bobrow M
Counselling following diagnosis of a fetal abnormality: the differing approaches of obstetricians, clinical geneticists, and genetic nurses.
Journal of medical genetics 1994;31(11):864-7.
1994: Muntoni F; Gobbi P; Sewry C; Sherratt T; Taylor J; Sandhu S K; Abbs S; Roberts R; Hodgson S V; Bobrow M
Deletions in the 5' region of dystrophin and resulting phenotypes.
Journal of medical genetics 1994;31(11):843-7.
1994: Davies A F; Barber L; Murer-Orlando M; Bobrow M; Adinolfi M
An improved method for the detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization.
Annals of the New York Academy of Sciences 1994;731():67-72.
1994: Flinter F; Boye E; Vetrie D; Harris A; Bobrow M
Genetic aspects of renal dysfunction: Alport's syndrome.
The Clinical investigator 1994;72(9):728.
1994: Davies A F; Barber L; Murer-Orlando M; Bobrow M; Adinolfi M
FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs.
Journal of medical genetics 1994;31(9):679-85.
1994: Bekker H; Denniss G; Modell M; Bobrow M; Marteau T
The impact of population based screening for carriers of cystic fibrosis.
Journal of medical genetics 1994;31(5):364-8.
1994: Vetrie D; Kendall E; Coffey A; Hassock S; Collins J; Todd C; Lehrach H; Bobrow M; Bentley D R; Harris A
A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22.
Genomics 1994;19(1):42-7.
1994: Marteau T; Drake H; Reid M; Feijoo M; Soares M; Nippert I; Nippert P; Bobrow M
Counselling following diagnosis of fetal abnormality: a comparison between German, Portuguese and UK geneticists.
European journal of human genetics : EJHG 1994;2(2):96-102.
1994: Roberts R G; Gardner R J; Bobrow M
Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations.
Human mutation 1994;4(1):1-11.
1993: Holding C; Bentley D; Roberts R; Bobrow M; Mathew C
Development and validation of laboratory procedures for preimplantation diagnosis of Duchenne muscular dystrophy.
Journal of medical genetics 1993;30(11):903-9.
1993: Wang Q; Green E; Barnicoat A; Garrett D; Mullarkey M; Bobrow M; Mathew C G
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndrome.
Lancet 1993;342(8878):1025-6.
1993: Vetrie D; Bentley D; Bobrow M; Harris A
Physical mapping shows close linkage between the alpha-galactosidase A gene (GLA) and the DXS178 locus.
Human genetics 1993;92(1):95-9.
1993: Flinter F A; Vetrie D; Bobrow M
The implications of the cloning of the XLA gene.
Journal of the Royal College of Physicians of London 1993;27(3):233-5.
1993: Bekker H; Modell M; Denniss G; Silver A; Mathew C; Bobrow M; Marteau T
Uptake of cystic fibrosis testing in primary care: supply push or demand pull?
BMJ (Clinical research ed.) 1993;306(6892):1584-6.
1993: Landels E C; Green P M; Ellis I H; Fensom A H; Kaback M M; Lim-Steele J; Zeiger K; Levy N; Bobrow M
Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British Isles.
Journal of medical genetics 1993;30(6):479-81.
1993: Barnicoat A J; Docherty Z; Bobrow M
Where have all the fragile X boys gone?
Developmental medicine and child neurology 1993;35(6):532-9.
1993: Boye E; Flinter F A; Bobrow M; Harris A
An 8 bp deletion in exon 51 of the COL4A5 gene of an Alport syndrome patient.
Human molecular genetics 1993;2(5):595-6.
1993: Abbs S; Bobrow M
Report on the 16th ENMC workshop--carrier diagnosis of Duchenne and Becker muscular dystrophy.
Neuromuscular disorders : NMD 1993;3(3):241-2.
1993: Roberts R G; Coffey A J; Bobrow M; Bentley D R
Exon structure of the human dystrophin gene.
Genomics 1993;16(2):536-8.
1993: Vetrie D; Bobrow M; Harris A
Construction of a 5.2-megabase physical map of the human X chromosome at Xq22 using pulsed-field gel electrophoresis and yeast artificial chromosomes.
Genomics 1993;15(3):631-42.
1993: Hirst M C; Barnicoat A; Flynn G; Wang Q; Daker M; Buckle V J; Davies K E; Bobrow M
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
Human molecular genetics 1993;2(2):197-200.
1993: Vetrie D; Vorechovský I; Sideras P; Holland J; Davies A; Flinter F; Hammarström L; Kinnon C; Levinsky R; Bobrow M
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.
Nature 1993;361(6409):226-33.
1993: Yau S C; Roberts R G; Bobrow M; Mathew C G
Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.
Lancet 1993;341(8840):273-5.
1993: Roberts R G; Passos-Bueno M R; Bobrow M; Vainzof M; Zatz M
Point mutation in a Becker muscular dystrophy patient.
Human molecular genetics 1993;2(1):75-7.
1993: Roberts R G; Bentley D R; Bobrow M
Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcripts.
Human mutation 1993;2(4):293-9.
1992: Cole C G; Patel K; Shipley J; Sheer D; Bobrow M; Bentley D R; Dunham I
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification.
Genomics 1992;14(4):931-8.
1992: Vetrie D; Flinter F; Bobrow M; Harris A
Construction of a yeast artificial chromosome contig encompassing the human alpha 5(IV) collagen gene (COL4A5).
Genomics 1992;14(3):634-42.
1992: Berry A C; Docherty Z; Bobrow M
Abnormal chromosome complement after normal amniocentesis result.
Lancet 1992;340(8831):1361.
1992: Vetrie D; Boye E; Flinter F; Bobrow M; Harris A
DNA rearrangements in the alpha 5(IV) collagen gene (COL4A5) of individuals with Alport syndrome: further refinement using pulsed-field gel electrophoresis.
Genomics 1992;14(3):624-33.
1992: Cole C G; Dunham I; Coffey A J; Ross M T; Meier-Ewert S; Bobrow M; Bentley D R
A random STS strategy for construction of YAC contigs spanning defined chromosomal regions.
Genomics 1992;14(2):256-62.
1992: Vetrie D; Flinter F; Bobrow M; Harris A
X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene?
Journal of medical genetics 1992;29(9):663-6.
1992: Harris A; Collins J; Vetrie D; Cole C; Bobrow M
X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.
Journal of medical genetics 1992;29(9):608-14.
1992: Roberts R G; Coffey A J; Bobrow M; Bentley D R
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.
Genomics 1992;13(4):942-50.
1992: Landels E C; Green P M; Ellis I H; Fensom A H; Bobrow M
Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles.
Journal of medical genetics 1992;29(8):563-7.
1992: Differ A M; Bobrow M; Mathew C G
A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.
Human genetics 1992;89(6):689.
1992: Flinter F; Bobrow M
The molecular genetics of Alport syndrome: report of two workshops.
Journal of medical genetics 1992;29(5):352-3.
1992: Abbs S; Bobrow M
Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
Journal of medical genetics 1992;29(3):191-6.
1992: Roberts R G; Bobrow M; Bentley D R
Point mutations in the dystrophin gene.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(6):2331-5.
1992: Vetrie D; Flinter F; Bobrow M; Harris A
Long-range mapping of the gene for the human alpha 5(IV) collagen chain at Xq22-q23.
Genomics 1992;12(1):130-8.
1992: Cole C G; Abbs S J; Dubowitz V; Hodgson S V; Warner J; Merlini L; Bobrow M
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIII.
Neuromuscular disorders : NMD 1992;2(1):51-7.
1992: Hodgson S V; Abbs S; Clark S; Manzur A; Heckmatt J Z; Dubowitz V; Bobrow M
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability.
Neuromuscular disorders : NMD 1992;2(4):269-76.
1991: Boye E; Vetrie D; Flinter F; Buckle B; Pihlajaniemi T; Hamalainen E R; Myers J C; Bobrow M; Harris A
Major rearrangements in the alpha 5(IV) collagen gene in three patients with Alport syndrome.
Genomics 1991;11(4):1125-32.
1991: Yau S C; Roberts R G; Bentley D R; Mathew C G; Bobrow M
A MseI polymorphism in exon 48 of the dystrophin gene.
Nucleic acids research 1991;19(20):5803.
1991: Roberts R G; Barby T F; Manners E; Bobrow M; Bentley D R
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes.
American journal of human genetics 1991;49(2):298-310.
1991: Cole C G; Goodfellow P N; Bobrow M; Bentley D R
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR.
Genomics 1991;10(3):816-26.
1991: Blonden L A; Grootscholten P M; den Dunnen J T; Bakker E; Abbs S; Bobrow M; Boehm C; van Broeckhoven C; Baumbach L; Chamberlain J
242 breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread.
Genomics 1991;10(3):631-9.
1991: Abbs S; Yau S C; Clark S; Mathew C G; Bobrow M
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
Journal of medical genetics 1991;28(5):304-11.
1991: Landels E C; Ellis I H; Fensom A H; Green P M; Bobrow M
Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish population.
Journal of medical genetics 1991;28(3):177-80.
1991: Landels E C; Ellis I H; Bobrow M; Fensom A H
Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.
Journal of medical genetics 1991;28(2):101-9.
1990: Roberts R G; Bentley D R; Barby T F; Manners E; Bobrow M
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA.
Lancet 1990;336(8730):1523-6.
1990: Abbs S; Roberts R G; Mathew C G; Bentley D R; Bobrow M
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.
Genomics 1990;7(4):602-6.
1990: Roberts R G; Bobrow M; Bentley D R
A MaeIII polymorphism near the dystrophin gene promoter by restriction of amplified DNA.
Nucleic acids research 1990;18(5):1315.
1989: Hodgson S; Hart K; Abbs S; Heckmatt J; Rodillo E; Bobrow M; Dubowitz V
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.
Journal of medical genetics 1989;26(11):682-93.
1989: Roberts R G; Montandon A J; Bobrow M; Bentley D R
Detection of novel genetic markers by mismatch analysis.
Nucleic acids research 1989;17(15):5961-71.
1989: Hart K A; Abbs S; Bobrow M
Pathogenic and nonpathogenic deletions in two families with Duchenne muscular dystrophy.
American journal of medical genetics 1989;33(1):142-5.
1989: Benham F; Hart K; Crolla J; Bobrow M; Francavilla M; Goodfellow P N
A method for generating hybrids containing nonselected fragments of human chromosomes.
Genomics 1989;4(4):509-17.
1989: Sheridan R; Llerena J; Matkins S; Debenham P; Cawood A; Bobrow M
Fertility in a male with trisomy 21.
Journal of medical genetics 1989;26(5):294-8.
1989: Hart K A; Abbs S; Wapenaar M C; Cole C G; Hodgson S V; Bobrow M
Molecular deletions in the Duchenne/Becker muscular dystrophy gene.
Clinical genetics 1989;35(4):251-60.
1989: Flinter F A; Abbs S; Bobrow M
Localization of the gene for classic Alport syndrome.
Genomics 1989;4(3):335-8.
1989: Llerena J; Murer-Orlando M; McGuire M; Zahed L; Sheridan R J; Berry A C; Bobrow M
Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndrome.
Journal of medical genetics 1989;26(3):174-8.
1989: Zahed L; Murer-Orlando M; Bobrow M
The application of automated metaphase scanning to direct preparations of chorionic villi.
Prenatal diagnosis 1989;9(1):7-17.
1989: Roberts R G; Cole C G; Hart K A; Bobrow M; Bentley D R
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy.
Nucleic acids research 1989;17(2):811.
1989: Patel K; Leevers S; Abbs S; Hart K A; Heckmatt J Z; Bobrow M; Dubowitz V
Absence of dystrophin in Becker muscular dystrophy.
Lancet 1989;1(8628):47.
1988: Mutton D E; Chown K; Thomson L; Berry A C; Botcherby P K; Bobrow M
PRUFILE: a clinical and laboratory database for the genetics centre.
Clinical genetics 1988;34(4):209-18.
1988: Zahed L; Murer-Orlando M; Bobrow M
Cell cycle studies in chorionic villi.
Human genetics 1988;80(2):127-34.
1988: Flinter F A; Cameron J S; Chantler C; Houston I; Bobrow M
Genetics of classic Alport's syndrome.
Lancet 1988;2(8618):1005-7.
1988: Murer-Orlando M; Llerena J; McGuire M; Zahed L; Crolla J; Bobrow M; Sheridan R
Chromosome banding in direct preparations of chorionic villi.
Prenatal diagnosis 1988;8(6):461-9.
1988: Flinter F A; Bobrow M
The application of molecular biology to the prenatal diagnosis of renal disease.
Pediatric nephrology (Berlin, Germany) 1988;2(3):343-50.
1988: Harris A; Lankester S; Haan E; Beres J; Hulten M; Szollar J; Souttier L; Bobrow M
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localization.
Clinical genetics 1988;34(1):1-6.
1988: Bobrow M
The prevention and avoidance of genetic disease: summing up.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;319(1194):361-7.
1988: Harris A; Quinlan C; Bobrow M
Cystic fibrosis typing with DNA probes: experience of a screening laboratory.
Human genetics 1988;79(1):76-9.
1988: Wapenaar M C; Kievits T; Hart K A; Abbs S; Blonden L A; den Dunnen J T; Grootscholten P M; Bakker E; Verellen-Dumoulin C; Bobrow M
A deletion hot spot in the Duchenne muscular dystrophy gene.
Genomics 1988;2(2):101-8.
1988: Cole C G; Walker A; Coyne A; Johnson L; Hart K A; Hodgson S; Sheridan R; Bobrow M
Prenatal testing for Duchenne and Becker muscular dystrophy.
Lancet 1988;1(8580):262-6.
1988: Bobrow M; Walker A; Walton J
The parental origin of mutations causing Duchenne muscular dystrophy.
Archives of neurology 1988;45(1):85-7.
1987: Hodgson S; Walker A; Cole C; Hart K; Johnson L; Heckmatt J; Dubowitz V; Bobrow M
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
Journal of medical genetics 1987;24(3):152-9.
1987: Hart K A; Hodgson S; Walker A; Cole C G; Johnson L; Dubowitz V; Bobrow M
DNA deletions in mild and severe Becker muscular dystrophy.
Human genetics 1987;75(3):281-5.
1986: Hart K; Cole C; Walker A; Hodgson S; Johnson L; Dubowitz V; Ray P; Worton R; Bobrow M
The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.
Journal of medical genetics 1986;23(6):516-20.
1986: Hodgson S; Boswinkel E; Cole C; Walker A; Dubowitz V; Granata C; Merlini L; Bobrow M
A linkage study of Emery-Dreifuss muscular dystrophy.
Human genetics 1986;74(4):409-16.
1986: Walker A; Hart K; Cole C; Hodgson S; Johnson L; Dubowitz V; Bobrow M
Linkage studies in Duchenne and Becker muscular dystrophies.
Journal of medical genetics 1986;23(6):538-47.
1986: Kunkel L M; Hejtmancik J F; Caskey C T; Speer A; Monaco A P; Middlesworth W; Colletti C A; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt S A; Bartlett R; Pericak-Vance M A; Roses A D; Thompson M W; Ray P N; Worton R G; Fischbeck K H; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan J C; Emery A; Dorkins H; McGlade S; Davies K E; Boehm C; Arveiler B; Lemaire C; Morgan G J; Denton M J; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox D E; Affara N A; Ferguson-Smith M A; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen G J; Pearson P L; Greenberg C R; Hamerton J L; Wrogemann K; Doherty R A; Polakowska R; Hyser C; Quirk S; Thomas N; Harper J F; Darras B T; Francke U
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature 1986;322(6074):73-7.
1986: Hodgson S; Hart K; Walker A; Cole C; Johnson L; Bobrow M; Dubowitz V; Kunkel L
DNA deletion in boy with Becker muscular dystrophy.
Lancet 1986;1(8486):918.
1985: Bobrow M
Heterochromatic chromosome variation and reproductive failure.
Experimental and clinical immunogenetics 1985;2(2):97-105.

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