S.-H. Chen

The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene

Qili Zhu, Miqin Zhang, R. Michael Blaese et al. · Blood · 1995 · 210 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

An intragenic deletion of the factor IX gene in a family with hemophilia B.

S.-H. Chen, Shigenori Yoshitake, P. F. Chance et al. · Journal of Clinical Investigation · 1985 · 47 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Factor IX mutations: Rapid, direct screening methods for 20 new families with hemophilia B

Arthur R. Thompson, Jon M. Schoof, Ann F. Weinmann et al. · Thrombosis Research · 1992 · 20 citations

Life Sciences, Genetics, Molecular Genetics +15

Studies on the human blood group p system: An existence of UDP-Gal:Lactosylceramide α1→4 galactosyltransferase in the small p type cells

Susumu Iizuka, S.-H. Chen, Akira Yoshida · Biochemical and Biophysical Research Communications · 1986 · 19 citations

Life Sciences, Biochemistry, Molecular Biology +8

The identification of a (CGG) 6 AGG insertion within the CGG repeat of the FMR1 gene in Asians

S.-H. Chen, Jonathan Schoof, Norman E. Buroker et al. · Human Genetics · 1997 · 19 citations

Life Sciences, Genetics, Molecular Genetics +5