J. Zonana

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

Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families.

Maurice Godfrey, Victor Menashe, Richard G. Weleber et al. · PubMed · 1990 · 93 citations

Life Sciences, Genetics, Molecular Genetics +6

Definitive Evidence for an Autosomal Recessive Form of Hypohidrotic Ectodermal Dysplasia Clinically Indistinguishable rom the More Common X-Linked Disorde

R. Munoz, G.G. Lestringant, Virginia P. Sybert et al. · The American Journal of Human Genetics · 1997 · 79 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene.

F Quan, J. Zonana, Kristine A. Gunter et al. · PubMed · 1995 · 69 citations

Life Sciences, Genetics, Molecular Genetics +11

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

J. Zonana, Alan R. Clarke, M. Sarfarazi et al. · PubMed · 1988 · 56 citations

Medicine, Genetics, Molecular Genetics +17