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T E Kelly

Showing results (71-80 of 103) with videos related to

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American Journal of Medical Genetics|June 1, 1985
Prenatal diagnosis of Pena-Shokeir syndrome type 1R H MacMillan, G M Harbert, W D Davis, et al.
Journal of Medical Genetics|May 11, 1991
Hypercoagulability in a patient with Marfan syndromeJ E Humphries, G A Stouffer, T E Kelly, et al.
American Journal of Medical Genetics|October 21, 1999
Expansion of a 27 CAG repeat allele into a symptomatic huntington disease-producing alleleT E Kelly, P Allinson, R C McGlennen, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1982
Craniofrontonasal dysplasia in a three-generation kindredJ F Reynolds, R J Haas, M T Edgerton, et al.
The Journal of Pediatrics|April 1, 1977
Gonadal dysgenesis with 45,XO/46,XX mosaicism demonstrated only in a streak gonadD E Goldstein, T E Kelly, A J Johanson, et al.
American Journal of Medical Genetics|July 9, 1999
Mosaicism in Prader-Willi syndrome: detection using fluorescent in situ hybridizationW L Golden, K W Sudduth, S H Burnett, et al.
Pediatrics|April 1, 1983
Dyskeratosis congenita: two examples of this multisystem disorderR Womer, J E Clark, P Wood, et al.
American Journal of Medical Genetics|November 1, 1984
Teratogenicity of anticonvulsant drugs. II: A prospective studyT E Kelly, P Edwards, M Rein, et al.
Virginia Medical|April 1, 1983
Fragile X-linked mental retardation, a new entity: case reportsT E Kelly, M A Shires, L Harris, et al.
Annals of Saudi Medicine|July 1, 1996
The genetics of the human growth hormone axis and associated dwarfing disordersT E Kelly, R Al-Saif, N Attia, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|June 1, 1985
Prenatal diagnosis of Pena-Shokeir syndrome type 1R H MacMillan, G M Harbert, W D Davis, et al.
Journal of Medical Genetics|May 11, 1991
Hypercoagulability in a patient with Marfan syndromeJ E Humphries, G A Stouffer, T E Kelly, et al.
American Journal of Medical Genetics|October 21, 1999
Expansion of a 27 CAG repeat allele into a symptomatic huntington disease-producing alleleT E Kelly, P Allinson, R C McGlennen, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1982
Craniofrontonasal dysplasia in a three-generation kindredJ F Reynolds, R J Haas, M T Edgerton, et al.
The Journal of Pediatrics|April 1, 1977
Gonadal dysgenesis with 45,XO/46,XX mosaicism demonstrated only in a streak gonadD E Goldstein, T E Kelly, A J Johanson, et al.
American Journal of Medical Genetics|July 9, 1999
Mosaicism in Prader-Willi syndrome: detection using fluorescent in situ hybridizationW L Golden, K W Sudduth, S H Burnett, et al.
Pediatrics|April 1, 1983
Dyskeratosis congenita: two examples of this multisystem disorderR Womer, J E Clark, P Wood, et al.
American Journal of Medical Genetics|November 1, 1984
Teratogenicity of anticonvulsant drugs. II: A prospective studyT E Kelly, P Edwards, M Rein, et al.
Virginia Medical|April 1, 1983
Fragile X-linked mental retardation, a new entity: case reportsT E Kelly, M A Shires, L Harris, et al.
Annals of Saudi Medicine|July 1, 1996
The genetics of the human growth hormone axis and associated dwarfing disordersT E Kelly, R Al-Saif, N Attia, et al.
Pageof 11