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American Journal of Medical Genetics
|
April 1, 1988
Report of two cases of distal deletion of the long arm of chromosome 6
C A Stevens, R M Fineman, W R Breg, et al.
Human Genetics
|
April 7, 1977
Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15
R R Schreck, W R Breg, B F Erlanger, et al.
Journal of the National Cancer Institute
|
August 1, 1981
Homogeneously staining region in a retinoblastoma cell line: relevance to tumor initiation and progression
F Gilbert, G Balaban, W R Breg, et al.
American Journal of Medical Genetics
|
May 1, 1990
Duplication of euchromatin without phenotypic effects: a variant of chromosome 16
C R Bryke, W R Breg, V R Potluri, et al.
Human Genetics
|
January 1, 1981
Evidence for methylation of inactive human rRNA genes in amplified regions
U Tantravahi, W R Breg, V Wertelecki, et al.
Pediatrics
|
April 1, 1978
Chromosome 3 duplication q/deletion p syndrome
R M Fineman, F Hecht, R C Ablow, et al.
American Journal of Human Genetics
|
November 1, 1984
A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis
K J Blakemore, M S Watson, J Samuelson, et al.
Clinical Genetics
|
September 1, 1993
Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome
M G Butler, R Pratesi, M S Watson, et al.
Pediatrics
|
November 1, 1975
Trisomy 8 mosaicism syndrome
R M Fineman, R C Ablow, R O Howard, et al.
Cytogenetics and Cell Genetics
|
January 1, 1976
Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870
W R Breg, M M Aronson, R Hill, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 87) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
April 1, 1988
Report of two cases of distal deletion of the long arm of chromosome 6
C A Stevens, R M Fineman, W R Breg, et al.
Human Genetics
|
April 7, 1977
Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15
R R Schreck, W R Breg, B F Erlanger, et al.
Journal of the National Cancer Institute
|
August 1, 1981
Homogeneously staining region in a retinoblastoma cell line: relevance to tumor initiation and progression
F Gilbert, G Balaban, W R Breg, et al.
American Journal of Medical Genetics
|
May 1, 1990
Duplication of euchromatin without phenotypic effects: a variant of chromosome 16
C R Bryke, W R Breg, V R Potluri, et al.
Human Genetics
|
January 1, 1981
Evidence for methylation of inactive human rRNA genes in amplified regions
U Tantravahi, W R Breg, V Wertelecki, et al.
Pediatrics
|
April 1, 1978
Chromosome 3 duplication q/deletion p syndrome
R M Fineman, F Hecht, R C Ablow, et al.
American Journal of Human Genetics
|
November 1, 1984
A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis
K J Blakemore, M S Watson, J Samuelson, et al.
Clinical Genetics
|
September 1, 1993
Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome
M G Butler, R Pratesi, M S Watson, et al.
Pediatrics
|
November 1, 1975
Trisomy 8 mosaicism syndrome
R M Fineman, R C Ablow, R O Howard, et al.
Cytogenetics and Cell Genetics
|
January 1, 1976
Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870
W R Breg, M M Aronson, R Hill, et al.
Page
of 9