Michael B. Petersen

Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker

Michael B. Petersen, Effrosini P. Economou, Susan A. Slaugenhaupt et al. · Genomics · 1990 · 59 citations · Full text

Cytogenetics, Genetic Disorder, Genetics +12

Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome

Michael B. Petersen, Georgia Karadima, Maria Samaritaki et al. · American Journal of Medical Genetics · 2000 · 35 citations

Down Syndrome, Alzheimer's Disease, Developmental Biology +10

Linkage mapping of highly informative DNA polymorphisms within the human interferon-α receptor gene on chromosome 21

Melvin G. McInnis, Georges Lutfalla, Susan Slaugenhaupt et al. · Genomics · 1991 · 32 citations · Full text

A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region

Oliver Bartsch, Georg Klaus Hinkel, Michael B. Petersen et al. · Human Genetics · 1997 · 20 citations

Down Syndrome, Developmental Biology, Genetic Disorder +8

Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10; 17) may indicate candidate gene regions

Anne‐Marie Gerdes, Michael B. Petersen, Henrik Daa Schrøder et al. · Clinical Genetics · 1994 · 15 citations

Congenital Myopathy, Genetics, Genetic Epidemiology +16