A R Brothman|D L Persons|L G Shaffer - JoVE Visualize

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Journal of Pediatric Hematology/Oncology|December 18, 1998

Lipoblastoma presenting as a mesenteric mass in an infantY Posey, E Valdivia, D L Persons, et al.

Genomics|April 1, 1993

A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: further studies on Robertsonian translocationsP Kalitsis, E Earle, B Vissel, 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.

Human Molecular Genetics|February 1, 1995

Further evidence that CENP-C is a necessary component of active centromeres: studies of a dic(X; 15) with simultaneous immunofluorescence and FISHS L Page, W C Earnshaw, K H Choo, et al.

Clinical Genetics|October 12, 1999

Molecular and clinical characterization of a patient with duplication of 1p36.3 and metopic synostosisH A Heilstedt, S K Shapira, A R Gregg, et al.

American Journal of Medical Genetics|March 31, 1997

Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratoryL G Shaffer, G M Kennedy, A S Spikes, et al.

Clinical Genetics|November 18, 2003

Omphalocele in trisomy 3q: further delineation of phenotypeS A Yatsenko, R Mendoza-Londono, J W Belmont, 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.

American Journal of Human Genetics|May 1, 1995

Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndromeE Nickerson, F Greenberg, M T Keating, et al.

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Showing results (101-110 of 215) with videos related to

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Pageof 22

Journal of Pediatric Hematology/Oncology|December 18, 1998

Lipoblastoma presenting as a mesenteric mass in an infantY Posey, E Valdivia, D L Persons, et al.

Genomics|April 1, 1993

A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: further studies on Robertsonian translocationsP Kalitsis, E Earle, B Vissel, 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.

Human Molecular Genetics|February 1, 1995

Further evidence that CENP-C is a necessary component of active centromeres: studies of a dic(X; 15) with simultaneous immunofluorescence and FISHS L Page, W C Earnshaw, K H Choo, et al.

Clinical Genetics|October 12, 1999

Molecular and clinical characterization of a patient with duplication of 1p36.3 and metopic synostosisH A Heilstedt, S K Shapira, A R Gregg, et al.

American Journal of Medical Genetics|March 31, 1997

Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratoryL G Shaffer, G M Kennedy, A S Spikes, et al.

Clinical Genetics|November 18, 2003

Omphalocele in trisomy 3q: further delineation of phenotypeS A Yatsenko, R Mendoza-Londono, J W Belmont, 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.

American Journal of Human Genetics|May 1, 1995

Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndromeE Nickerson, F Greenberg, M T Keating, et al.

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