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J A Crolla

Showing results (41-50 of 78) with videos related to

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Human Genetics|February 1, 1995
Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosisJ A Crolla, J F Harvey, F L Sitch, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
A search for uniparental disomy in carriers of supernumerary marker chromosomesR S James, I K Temple, N R Dennis, et al.
Archives of Medical Research|April 18, 2000
Functional Xp disomy and hypomelanosis of ItoH Rivera, L S Correa-Cerro, D O Robinson, et al.
Human Genetics|January 1, 1995
Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletionsD J Bunyan, J A Crolla, A L Collins, et al.
Human Genetics|December 22, 1999
Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical regionN S Thomas, C E Browne, C Oley, et al.
American Journal of Medical Genetics|December 31, 1997
A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomesJ A Crolla, P Howard, C Mitchell, et al.
American Journal of Human Genetics|June 4, 2026
Patricia A. Jacobs (1934-2026)S Ennis, S L Sherman, T J Hassold, et al.
American Journal of Human Genetics|October 16, 2003
Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexityS E Roberts, F Maggouta, N S Thomas, et al.
Genetic Counseling (Geneva, Switzerland)|November 21, 2007
A de novo (1;2;3;15;18) chromosome rearrangement with six nonreciprocal translocationsH Rivera, M G Domínguez, J A Crolla, et al.
Journal of Medical Genetics|June 1, 1996
Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23)A E Cockwell, R S James, I E Moore, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
Human Genetics|February 1, 1995
Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosisJ A Crolla, J F Harvey, F L Sitch, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
A search for uniparental disomy in carriers of supernumerary marker chromosomesR S James, I K Temple, N R Dennis, et al.
Archives of Medical Research|April 18, 2000
Functional Xp disomy and hypomelanosis of ItoH Rivera, L S Correa-Cerro, D O Robinson, et al.
Human Genetics|January 1, 1995
Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletionsD J Bunyan, J A Crolla, A L Collins, et al.
Human Genetics|December 22, 1999
Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical regionN S Thomas, C E Browne, C Oley, et al.
American Journal of Medical Genetics|December 31, 1997
A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomesJ A Crolla, P Howard, C Mitchell, et al.
American Journal of Human Genetics|June 4, 2026
Patricia A. Jacobs (1934-2026)S Ennis, S L Sherman, T J Hassold, et al.
American Journal of Human Genetics|October 16, 2003
Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexityS E Roberts, F Maggouta, N S Thomas, et al.
Genetic Counseling (Geneva, Switzerland)|November 21, 2007
A de novo (1;2;3;15;18) chromosome rearrangement with six nonreciprocal translocationsH Rivera, M G Domínguez, J A Crolla, et al.
Journal of Medical Genetics|June 1, 1996
Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23)A E Cockwell, R S James, I E Moore, et al.
Pageof 8