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Publications by M Bobrow

Accurate Diagnosis of Carriers of Deletions and Duplications in Duchenne/Becker Muscular Dystrophy by Fluorescent Dosage Analysis.

Journal of Medical Genetics
Genetics
1996English

Analysis of Quantitative PCR for the Diagnosis of Deletion and Duplication Carriers in the Dystrophin Gene.

Journal of Medical Genetics
Genetics
1992English

Deletions in the 5' Region of Dystrophin and Resulting Phenotypes.

Journal of Medical Genetics
Genetics
1994English

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
Genetics
1989English

Tay-Sachs Disease Heterozygote Detection: Use of a Centrifugal Analyser for Automation of Hexosaminidase Assays With Two Different Artificial Substrates.

Journal of Medical Genetics
Genetics
1991English

Fertility in a Male With Trisomy 21.

Journal of Medical Genetics
Genetics
1992English

Beta-Hexosaminidase Splice Site Mutation Has a High Frequency Among Non-Jewish Tay-Sachs Disease Carriers From the British Isles.

Journal of Medical Genetics
Genetics
1992English

Clinical, Cytogenetic, and Molecular Analysis of Three Families With FRAXE.

Journal of Medical Genetics
Genetics
1997English

Better Quality Data for Down's Syndrome Register.

BMJ
1993English

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