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American Journal of Human Genetics|March 1, 1995
Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton functionK Stephens, A Zlotogorski, L Smith, et al.The Journal of Investigative Dermatology|January 1, 1990
Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: variable morphology and structural protein expression and a defect in lamellar granulesB A Dale, K A Holbrook, P Fleckman, et al.The Journal of Investigative Dermatology|June 16, 2001
Expression of a truncated keratin 5 may contribute to severe palmar--plantar hyperkeratosis in epidermolysis bullosa simplex patientsR J Livingston, V P Sybert, L T Smith, et al.American Journal of Medical Genetics|May 3, 1996
Arthrogryposis associated with unsuccessful attempts at termination of pregnancyJ G HallImmunology|September 1, 1984
Studies on the adjuvant action of beryllium. I. Effects on individual lymph nodesJ G HallJournal of Medical Genetics|July 1, 1988
The value of the study of natural history in genetic disorders and congenital anomaly syndromesJ G HallJournal of Pediatric Orthopedics. Part B|July 1, 1997
Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspectsJ G HallDevelopment (Cambridge, England). Supplement|January 1, 1990
How imprinting is relevant to human diseaseJ G HallPageof 30