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

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International Journal of Cancer|September 1, 1994

Tumorigenicity of SV40 T antigen immortalized human prostate epithelial cells: association with decreased epidermal growth factor receptor (EGFR) expressionV L Bae, C K Jackson-Cook, A R Brothman, et al.

American Journal of Medical Genetics|October 21, 1998

Systematic search for uniparental disomy in early fetal losses: the results and a review of the literatureL G Shaffer, C McCaskill, K Adkins, et al.

American Journal of Human Genetics|April 25, 2000

Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomesS A Berend, J Horwitz, C McCaskill, et al.

The Journal of Reproductive Medicine|May 1, 1996

Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case reportL G Shaffer, A S Spikes, M Macha, et al.

The Journal of Urology|October 1, 1994

Chromosomal aneusomies detected by fluorescent in situ hybridization analysis in clinically localized prostate carcinomaJ A Brown, A Alcaraz, S Takahashi, et al.

Nature Genetics|March 1, 1995

Mutation of the MXI1 gene in prostate cancerL R Eagle, X Yin, A R Brothman, et al.

Neurology|December 1, 1992

Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.

American Journal of Medical Genetics|May 22, 1995

Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomaliesA S Spikes, K Hegmann, J L Smith, et al.

Clinical Genetics|December 1, 1996

Silver-Russell syndrome and exclusion of uniparental disomyM L Ayala-Madrigal, L G Shaffer, M L Ramírez-Dueñas

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.

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Showing results (81-90 of 215) with videos related to

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Pageof 22

International Journal of Cancer|September 1, 1994

Tumorigenicity of SV40 T antigen immortalized human prostate epithelial cells: association with decreased epidermal growth factor receptor (EGFR) expressionV L Bae, C K Jackson-Cook, A R Brothman, et al.

American Journal of Medical Genetics|October 21, 1998

Systematic search for uniparental disomy in early fetal losses: the results and a review of the literatureL G Shaffer, C McCaskill, K Adkins, et al.

American Journal of Human Genetics|April 25, 2000

Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomesS A Berend, J Horwitz, C McCaskill, et al.

The Journal of Reproductive Medicine|May 1, 1996

Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case reportL G Shaffer, A S Spikes, M Macha, et al.

The Journal of Urology|October 1, 1994

Chromosomal aneusomies detected by fluorescent in situ hybridization analysis in clinically localized prostate carcinomaJ A Brown, A Alcaraz, S Takahashi, et al.

Nature Genetics|March 1, 1995

Mutation of the MXI1 gene in prostate cancerL R Eagle, X Yin, A R Brothman, et al.

Neurology|December 1, 1992

Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.

American Journal of Medical Genetics|May 22, 1995

Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomaliesA S Spikes, K Hegmann, J L Smith, et al.

Clinical Genetics|December 1, 1996

Silver-Russell syndrome and exclusion of uniparental disomyM L Ayala-Madrigal, L G Shaffer, M L Ramírez-Dueñas

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.

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