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C D Kashork

Showing results (1-10 of 19) with videos related to

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American Journal of Human Genetics|October 18, 2000
The promise and pitfalls of telomere region-specific probesB C Ballif, C D Kashork, L G Shaffer
Prenatal Diagnosis|June 9, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridizationC D Kashork, J R Lupski, L G Shaffer
European Journal of Human Genetics : EJHG|October 20, 2000
FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probesB C Ballif, C D Kashork, L G Shaffer
Cytogenetic and Genome Research|September 7, 2006
Rearrangements of chromosome 18 illustrate the utility of array-based comparative genomic hybridizationC D Kashork, A Theisen, B A Bejjani, et al.
American Journal of Medical Genetics|July 16, 1999
Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to the LIS1 and the D17S379 lociO M Mutchinick, L G Shaffer, C D Kashork, et al.
American Journal of Medical Genetics|June 8, 2000
Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probesC A Bacino, C D Kashork, N A Davino, et al.
American Journal of Medical Genetics|November 24, 1999
Caution: telomere crossingL G Shaffer, C D Kashork, C A Bacino, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1AC D Kashork, K S Chen, J R Lupski, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approachA H Ligon, C D Kashork, C S Richards, et al.
Clinical Genetics|September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormalityH A Heilstedt, B C Ballif, L A Howard, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|October 18, 2000
The promise and pitfalls of telomere region-specific probesB C Ballif, C D Kashork, L G Shaffer
Prenatal Diagnosis|June 9, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridizationC D Kashork, J R Lupski, L G Shaffer
European Journal of Human Genetics : EJHG|October 20, 2000
FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probesB C Ballif, C D Kashork, L G Shaffer
Cytogenetic and Genome Research|September 7, 2006
Rearrangements of chromosome 18 illustrate the utility of array-based comparative genomic hybridizationC D Kashork, A Theisen, B A Bejjani, et al.
American Journal of Medical Genetics|July 16, 1999
Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to the LIS1 and the D17S379 lociO M Mutchinick, L G Shaffer, C D Kashork, et al.
American Journal of Medical Genetics|June 8, 2000
Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probesC A Bacino, C D Kashork, N A Davino, et al.
American Journal of Medical Genetics|November 24, 1999
Caution: telomere crossingL G Shaffer, C D Kashork, C A Bacino, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1AC D Kashork, K S Chen, J R Lupski, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approachA H Ligon, C D Kashork, C S Richards, et al.
Clinical Genetics|September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormalityH A Heilstedt, B C Ballif, L A Howard, et al.
Pageof 2