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Birth Defects Original Article Series
|
January 1, 1990
Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973
J A Evans, R de von Flindt, C R Greenberg, et al.
Human Genetics
|
January 1, 1982
Homozygous Robertsonian translocations in a fetus with 44 chromosomes
C 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-qter
N 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 syndrome
C 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 dystrophy
R G Thompson, E S Sponder, E Rosenmann, et al.
Nucleic Acids Research
|
July 25, 1989
TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7
Y Myal, C A Gregory, C Karpan, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Cytogenetic characteristics of 26 polyethylene glycol-induced human-hamster hybrid cell lines
H 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 sizes
S 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 anomalies
J 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 site
R G Thompson, B Nickel, S Finlayson, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 116) with videos related to
Sort By:
Page
of 12
Birth Defects Original Article Series
|
January 1, 1990
Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973
J A Evans, R de von Flindt, C R Greenberg, et al.
Human Genetics
|
January 1, 1982
Homozygous Robertsonian translocations in a fetus with 44 chromosomes
C 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-qter
N 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 syndrome
C 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 dystrophy
R G Thompson, E S Sponder, E Rosenmann, et al.
Nucleic Acids Research
|
July 25, 1989
TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7
Y Myal, C A Gregory, C Karpan, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Cytogenetic characteristics of 26 polyethylene glycol-induced human-hamster hybrid cell lines
H 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 sizes
S 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 anomalies
J 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 site
R G Thompson, B Nickel, S Finlayson, et al.
Page
of 12