S Toth-Fejel

Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

R.E. Magenis, S Toth-Fejel, Leland Allen et al. · American Journal of Medical Genetics · 1990 · 198 citations

Life Sciences, Genetics, Cytogenetics +14

Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy.

F Quan, Jadwiga Janas, S Toth-Fejel et al. · PubMed · 1997 · 99 citations

Life Sciences, Genetics, Molecular Genetics +13

Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1 ? q22.3 in a patient with tyrosinemia type II

E. Natt, Eva-Maria Westphal, S Toth-Fejel et al. · Human Genetics · 1987 · 73 citations

Life Sciences, Genetics, Molecular Genetics +10

The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13.

C. D. Boyd, S Toth-Fejel, Inder Gadi et al. · PubMed · 1988 · 44 citations

Life Sciences, Genetics, Molecular Genetics +7

Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization.

R.E. Magenis, James F. Gusella, Karen Weliky et al. · PubMed · 1986 · 41 citations

Life Sciences, Genetics, Molecular Genetics +13