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Indian Journal of Dermatology, Venereology and Leprology|October 6, 2010
Nail changes in systemic diseases : A clinical study of 435 casesS Abraham, N Kamath, G S Pai, et al.
In Vitro|April 1, 1981
Characterization of newly established human osteosarcoma cell line, LM-1K Y Tsang, G S Pai, H H Fudenberg
Annals of Clinical and Laboratory Science|January 1, 1995
An atypical Turner syndrome patient with ring X chromosome mosaicismE S Cantú, D F Jacobs, G S Pai
American Journal of Human Genetics|February 1, 1990
Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblastsD M DeBauche, G S Pai, W S Stanley
Cancer Genetics and Cytogenetics|May 1, 1992
Heterozygote detection through bleomycin-induced G2 chromatid breakage in dyskeratosis congenita familiesY Ning, Y Yongshan, G S Pai, et al.
American Journal of Medical Genetics|November 6, 1995
X-linked myotubular myopathy: clinical observations in ten additional casesM Joseph, G S Pai, K R Holden, et al.
Clinical Dysmorphology|January 11, 2001
Ischiospinal dysostosis with rib gaps and nephroblastomatosisJ Spranger, S Self, K B Clarkson, et al.
Indian Journal of Dermatology, Venereology and Leprology|July 24, 2007
Cutaneous manifestations of non-Hodgkin's lymphomaS S Kumar, M Kuruvilla, G S Pai, et al.
Annals of Neurology|October 1, 1992
Paternal uniparental disomy of chromosome 15 in a child with Angelman syndromeR D Nicholls, G S Pai, W Gottlieb, et al.
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