Kathi Marymee

Simpson-Golabi-Behmel syndrome: Genotype/phenotype analysis of 18 affected males from 7 unrelated families

R Hughes-Benzie, Giuseppe Pilia, J.Y. Xuan et al. · American Journal of Medical Genetics · 1996 · 136 citations

Life Sciences, Genetics, Molecular Genetics +15

GeneTests-GeneClinics: Genetic testing information for a growing audience

Roberta A Pagon, Peter Tarczy‐Hornoch, Patricia K. Baskin et al. · Human Mutation · 2002 · 83 citations

Life Sciences, Genetics, Molecular Genetics +13

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

Development of the Critical Elements of Genetic Evaluation and Genetic Counseling for Genetic Professionals and Perinatologists in Washington State

Kathi Marymee, Cynthia R. Dolan, Roberta A Pagon et al. · Journal of Genetic Counseling · 1998 · 13 citations · Full text

Life Sciences, Genetics, Genetic Counseling +11

Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis

Jonathan Zonana, Mansoor Sarfarazi, N S Thomas et al. · The Journal of Pediatrics · 1989 · 12 citations

Life Sciences, Genetics, Molecular Genetics +13