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Journal of the American Academy of Dermatology|October 1, 1991
Sipple syndrome with lichen amyloidosis as a paracrinopathy: pleiotropy, heterogeneity, or a contiguous gene?B G Kousseff, C Espinoza, G A ZamoreAmerican 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|February 1, 1992
Ankyloblepharon filiforme adnatumA H Weiss, G Riscile, B G KousseffAmerican Journal of Medical Genetics|January 30, 1995
Clitoromegaly in neurofibromatosisR Sutphen, E Galán-Goméz, B G KousseffProgress in Clinical and Biological Research|January 1, 1976
Growth hormone and prolactin in the fetusA W RootCritical Reviews in Clinical Laboratory Sciences|July 14, 2000
Genetic disorders of calcium and phosphorus metabolismA W RootJournal of Endocrinological Investigation|January 1, 1989
Neurophysiological regulation of the secretion of growth hormoneA W RootActa Paediatrica Scandinavica|January 1, 1991
Unique brain anomalies in an infant of a diabetic motherB G Kousseff, C Villaveces, C R MartinezThe Journal of Pediatrics|February 1, 1994
Free triiodothyronine toxicosis in two adolescentsA W RootAmerican Journal of Medical Genetics|September 1, 1985
Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vesselsM A Gieron, J K Korthals, B G KousseffPageof 14