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C R Bryke

Showing results (1-10 of 11) with videos related to

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American Journal of Medical Genetics|October 1, 1989
Antenatal diagnosis of 45,X/48,XYYYC R Bryke, M J Mahoney, T L Yang-Feng
American Journal of Medical Genetics|June 1, 1990
Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2])C R Bryke, V Lindgren, J S Fryburg, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 1, 1985
Solitary rectal ulcer syndrome in a teenaged boyJ M Sondheimer, T A Slagle, C R Bryke, et al.
Pediatrics|November 1, 1988
Pediatric residencies: differences between 1959/1960 and 1984/1985C R Bryke, W W Tunnessen, T J Scully, et al.
American Journal of Human Genetics|May 1, 1992
Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposisV Lindgren, C R Bryke, T Ozcelik, et al.
American Journal of Medical Genetics|May 1, 1990
Duplication of euchromatin without phenotypic effects: a variant of chromosome 16C R Bryke, W R Breg, V R Potluri, et al.
Human Genetics|February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypesV Lindgren, C P Chen, C R Bryke, et al.
American Journal of Medical Genetics|August 1, 1994
Desbuquois syndrome: clinical, radiographic, and morphologic characterizationM Shohat, R Lachman, H E Gruber, et al.
Cancer Research|April 15, 1987
Small cell lung cancer cell line derived from a primary tumor with a characteristic deletion of 3pS L Graziano, B Y Cowan, D N Carney, et al.
American Journal of Human Genetics|October 31, 2000
Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotypeG A Bellus, E B Spector, P W Speiser, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|October 1, 1989
Antenatal diagnosis of 45,X/48,XYYYC R Bryke, M J Mahoney, T L Yang-Feng
American Journal of Medical Genetics|June 1, 1990
Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2])C R Bryke, V Lindgren, J S Fryburg, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 1, 1985
Solitary rectal ulcer syndrome in a teenaged boyJ M Sondheimer, T A Slagle, C R Bryke, et al.
Pediatrics|November 1, 1988
Pediatric residencies: differences between 1959/1960 and 1984/1985C R Bryke, W W Tunnessen, T J Scully, et al.
American Journal of Human Genetics|May 1, 1992
Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposisV Lindgren, C R Bryke, T Ozcelik, et al.
American Journal of Medical Genetics|May 1, 1990
Duplication of euchromatin without phenotypic effects: a variant of chromosome 16C R Bryke, W R Breg, V R Potluri, et al.
Human Genetics|February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypesV Lindgren, C P Chen, C R Bryke, et al.
American Journal of Medical Genetics|August 1, 1994
Desbuquois syndrome: clinical, radiographic, and morphologic characterizationM Shohat, R Lachman, H E Gruber, et al.
Cancer Research|April 15, 1987
Small cell lung cancer cell line derived from a primary tumor with a characteristic deletion of 3pS L Graziano, B Y Cowan, D N Carney, et al.
American Journal of Human Genetics|October 31, 2000
Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotypeG A Bellus, E B Spector, P W Speiser, et al.
Pageof 2