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American Journal of Medical Genetics|June 27, 1997
Expanded phenotype of cranioectodermal dysplasia (Sensenbrenner syndrome)M J Amar, R Sutphen, B G KousseffAmerican Journal of Medical Genetics|July 3, 1995
XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome)R Sutphen, M J Amar, B G Kousseff, et al.American Journal of Medical Genetics|January 30, 1995
Clitoromegaly in neurofibromatosisR Sutphen, E Galán-Goméz, B G KousseffClinical Genetics|August 1, 1995
Tracheoesophageal anomalies in oculoauriculovertebral (Goldenhar) spectrumR Sutphen, E Galan-Gomez, X Cortada, et al.American Journal of Medical Genetics|August 14, 1995
Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothersO T Mueller, J K Hartsfield, M J Amar, et al.American Journal of Medical Genetics|January 1, 1981
Cohen syndrome: further delineation and inheritanceB G KousseffClinical Genetics|February 1, 1990
The phakomatoses as paracrine growth disorders (paracinopathies)B G KousseffAmerican Journal of Medical Genetics|December 1, 1982
The cytogenetic controversy in the Prader-Labhart-Willi syndromeB G KousseffPageof 8