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W R Breg

Showing results (11-20 of 87) with videos related to

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Lancet (London, England)|June 12, 1971
Fluorescence and Y translocation in XX malesW R Breg, G M Dillard, E M Short
Journal of Medical Genetics|March 1, 1974
Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus)Y M Wright, W E Clark, W R Breg
Cancer Genetics and Cytogenetics|July 1, 1984
Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaicM Nieneltow, M Cooper, W R Breg, et al.
Journal of Medical Genetics|September 1, 1972
A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brotherE M Short, G B Solitare, W R Breg
Journal of Medical Genetics|December 1, 1974
21 monosomy in a retarded female infantK H Halloran, W R Breg, M J Mahoney
Blood|September 1, 1979
Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasiaB Cooper, P V Tishler, L Atkins, et al.
Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.
American Journal of Medical Genetics|January 1, 1979
Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two familiesR M Liberfarb, W R Breg, L Atkins, et al.
Human Genetics|January 1, 1980
H-Y antigen in X,i(Xq) gonadal dysgenesis: evidence of X-linked genes in testicular differentiationS S Wachtel, G C Koo, W R Breg, et al.
Birth Defects Original Article Series|January 1, 1974
Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndromeY E Hsia, V Appadorai, W R Breg, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Lancet (London, England)|June 12, 1971
Fluorescence and Y translocation in XX malesW R Breg, G M Dillard, E M Short
Journal of Medical Genetics|March 1, 1974
Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus)Y M Wright, W E Clark, W R Breg
Cancer Genetics and Cytogenetics|July 1, 1984
Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaicM Nieneltow, M Cooper, W R Breg, et al.
Journal of Medical Genetics|September 1, 1972
A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brotherE M Short, G B Solitare, W R Breg
Journal of Medical Genetics|December 1, 1974
21 monosomy in a retarded female infantK H Halloran, W R Breg, M J Mahoney
Blood|September 1, 1979
Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasiaB Cooper, P V Tishler, L Atkins, et al.
Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.
American Journal of Medical Genetics|January 1, 1979
Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two familiesR M Liberfarb, W R Breg, L Atkins, et al.
Human Genetics|January 1, 1980
H-Y antigen in X,i(Xq) gonadal dysgenesis: evidence of X-linked genes in testicular differentiationS S Wachtel, G C Koo, W R Breg, et al.
Birth Defects Original Article Series|January 1, 1974
Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndromeY E Hsia, V Appadorai, W R Breg, et al.
Pageof 9