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Journal of Medical Genetics|December 1, 1982
A homozygote for pericentric inversion of chromosome 4N J Carpenter, B Say, N D BarberSouthern Medical Journal|September 1, 1987
Skeletal dysplasia in an infant with hypertelorism, hypospadias, developmental delay, and a complex chromosomal translocationB Say, N J CarpenterJournal of Medical Genetics|June 1, 1980
Gonadal dysgenesis in a patient with an X;3 translocation: case report and reviewN J Carpenter, B Say, D BrowningAmerican Journal of Diseases of Children (1960)|May 1, 1982
Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown originN J Carpenter, L G Leichtman, B SayJournal of Medical Genetics|December 1, 1980
Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+)B Say, N J Carpenter, G Giacoia, et al.Journal of Medical Genetics|June 1, 1981
An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?N J Carpenter, L G Leichtman, S Stamper, et al.Journal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.Journal of Medical Genetics|November 1, 1987
Partial deletion 21: case report with biochemical studies and reviewN J Carpenter, J S Mayes, B Say, et al.American Journal of Medical Genetics|July 31, 1995
Partial trisomy 13q identified by sequential fluorescence in situ hybridizationV V Rao, N J Carpenter, M Gucsavas, et al.Annales De Genetique|January 1, 1996
Familial deletion of chromosome 18 (p11.2)G V Velagaleti, S Harris, N J Carpenter, et al.Pageof 10