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J L HAMERTON

Showing results (21-30 of 45) with videos related to

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American Journal of Medical Genetics|September 15, 1991
Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypesA J Kirkilionis, A E Chudley, C A Gregory, et al.
Cytogenetics and Cell Genetics|January 1, 1986
The gene for clotting factor 10 is mapped to 13q32----qterN J Royle, M R Fung, R T MacGillivray, et al.
Human Genetics|January 1, 1982
Homozygous Robertsonian translocations in a fetus with 44 chromosomesC Rockman-Greenberg, M Ray, J A Evans, et al.
Somatic Cell and Molecular Genetics|March 1, 1988
Structural gene encoding human factor XII is located at 5q33-qterN J Royle, M Nigli, D Cool, et al.
Human Genetics|November 1, 1991
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndromeC A Gregory, J Schwartz, A J Kirkilionis, et al.
Journal of the Neurological Sciences|November 1, 1982
Proline incorporation by cultured skin fibroblasts from patients with duchenne muscular dystrophyR G Thompson, E S Sponder, E Rosenmann, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Cytogenetic characteristics of 26 polyethylene glycol-induced human-hamster hybrid cell linesH S Wang, V Niewczas, H R de S Nazareth, et al.
Cytogenetics and Cell Genetics|January 1, 1986
A DNA marker for human chromosome 8 that detects alleles of differing sizesS Wood, R Poon, D C Riddell, et al.
Birth Defects Original Article Series|January 1, 1982
A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomaliesJ A Evans, R de von Flindt, C Greenberg, et al.
Nature|August 25, 1983
56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy siteR G Thompson, B Nickel, S Finlayson, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|September 15, 1991
Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypesA J Kirkilionis, A E Chudley, C A Gregory, et al.
Cytogenetics and Cell Genetics|January 1, 1986
The gene for clotting factor 10 is mapped to 13q32----qterN J Royle, M R Fung, R T MacGillivray, et al.
Human Genetics|January 1, 1982
Homozygous Robertsonian translocations in a fetus with 44 chromosomesC Rockman-Greenberg, M Ray, J A Evans, et al.
Somatic Cell and Molecular Genetics|March 1, 1988
Structural gene encoding human factor XII is located at 5q33-qterN J Royle, M Nigli, D Cool, et al.
Human Genetics|November 1, 1991
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndromeC A Gregory, J Schwartz, A J Kirkilionis, et al.
Journal of the Neurological Sciences|November 1, 1982
Proline incorporation by cultured skin fibroblasts from patients with duchenne muscular dystrophyR G Thompson, E S Sponder, E Rosenmann, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Cytogenetic characteristics of 26 polyethylene glycol-induced human-hamster hybrid cell linesH S Wang, V Niewczas, H R de S Nazareth, et al.
Cytogenetics and Cell Genetics|January 1, 1986
A DNA marker for human chromosome 8 that detects alleles of differing sizesS Wood, R Poon, D C Riddell, et al.
Birth Defects Original Article Series|January 1, 1982
A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomaliesJ A Evans, R de von Flindt, C Greenberg, et al.
Nature|August 25, 1983
56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy siteR G Thompson, B Nickel, S Finlayson, et al.
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