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W R Breg

Showing results (61-70 of 87) with videos related to

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American Journal of Medical Genetics|October 1, 1982
H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesisF P Haseltine, V A Lynch, D L Van Dyke, et al.
Journal of Autism and Developmental Disorders|December 1, 1987
A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autismR Paul, E Dykens, J F Leckman, et al.
Somatic Cell and Molecular Genetics|March 1, 1986
Regional location of alpha 1-antichymotrypsin and alpha 1-antitrypsin genes on human chromosome 14M Rabin, M Watson, V Kidd, et al.
The Journal of Pediatrics|November 1, 1970
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)W R Breg, M W Steele, O J Miller, et al.
American Journal of Medical Genetics|March 1, 1986
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataW Wertelecki, W R Breg, J M Graham, et al.
Humangenetik|January 1, 1971
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescenceP W Allderdice, O J Miller, D A Miller, et al.
Transactions of the American Ophthalmological Society|January 1, 1978
Retinoblastoma and partial deletion of the long arm of chromosome 13R O Howard, D Warburton, W R Breg, et al.
Obstetrics and Gynecology|March 1, 1980
XY gonadal dysgenesis associated with the congenital nephrotic syndromeJ M Gertner, A Kauschansky, D W Giesker, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1984
Human c-fos oncogene mapped within chromosomal region 14q21----q31P E Barker, M Rabin, M Watson, et al.
American Journal of Medical Genetics|March 15, 1993
Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)E M Petty, L H Gibson, W R Breg, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|October 1, 1982
H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesisF P Haseltine, V A Lynch, D L Van Dyke, et al.
Journal of Autism and Developmental Disorders|December 1, 1987
A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autismR Paul, E Dykens, J F Leckman, et al.
Somatic Cell and Molecular Genetics|March 1, 1986
Regional location of alpha 1-antichymotrypsin and alpha 1-antitrypsin genes on human chromosome 14M Rabin, M Watson, V Kidd, et al.
The Journal of Pediatrics|November 1, 1970
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)W R Breg, M W Steele, O J Miller, et al.
American Journal of Medical Genetics|March 1, 1986
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataW Wertelecki, W R Breg, J M Graham, et al.
Humangenetik|January 1, 1971
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescenceP W Allderdice, O J Miller, D A Miller, et al.
Transactions of the American Ophthalmological Society|January 1, 1978
Retinoblastoma and partial deletion of the long arm of chromosome 13R O Howard, D Warburton, W R Breg, et al.
Obstetrics and Gynecology|March 1, 1980
XY gonadal dysgenesis associated with the congenital nephrotic syndromeJ M Gertner, A Kauschansky, D W Giesker, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1984
Human c-fos oncogene mapped within chromosomal region 14q21----q31P E Barker, M Rabin, M Watson, et al.
American Journal of Medical Genetics|March 15, 1993
Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)E M Petty, L H Gibson, W R Breg, et al.
Pageof 9