Fragile‐X syndrome III: Dermatoglyphic studies in males
Nancy E. Simpson(Queen's University), John M. Opitz(University of Utah), M. W. Partington(University of King's College), Bronwyn Newman(Queen's University)
Cited by 16
Related Papers
International nosology of heritable disorders of connective tissue, Berlin, 1986
|American Journal of Medical Genetics|1988|733
Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel‐Feil, and Möbius anomalies
|American Journal of Medical Genetics|1986|623
Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
|American Journal of Medical Genetics|1989|583
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
|Human Genetics|1985|512
Noonan syndrome: A review
|American Journal of Medical Genetics|1985|476