A M Goldstein|G W Reagan - JoVE Visualize

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Clinical Genetics|December 17, 2009

Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal developmentR Moslehi, C Signore, D Tamura, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 10, 1999

Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancerN Hu, M J Roth, M R Emmert-Buck, et al.

Pediatric Surgery International|June 16, 2019

Guidelines for the management of postoperative soiling in children with Hirschsprung diseaseP Saadai, A F Trappey, A M Goldstein, et al.

Carcinogenesis|November 4, 2000

High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern ChinaJ Huang, N Hu, A M Goldstein, et al.

Human Mutation|May 29, 1998

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutationsP M Pollock, N Spurr, T Bishop, et al.

Genes, Chromosomes & Cancer|July 4, 2001

Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinomaG Li, N Hu, A M Goldstein, et al.

The British Journal of Dermatology|December 3, 2020

Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneityR Laskar, A Ferreiro-Iglesias, D T Bishop, et al.

Anticancer Research|April 27, 1999

Familial and sporadic cases of nasopharyngeal carcinoma in TaiwanA Ung, C J Chen, P H Levine, et al.

Journal of Medical Genetics|June 7, 2005

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanomaK Laud, C Marian, M F Avril, et al.

Genes, Chromosomes & Cancer|February 19, 2000

Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese populationN Hu, M J Roth, M Polymeropolous, et al.

Pageof 15

Showing results (121-130 of 143) with videos related to

Sort By:

Pageof 15

Clinical Genetics|December 17, 2009

Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal developmentR Moslehi, C Signore, D Tamura, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 10, 1999

Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancerN Hu, M J Roth, M R Emmert-Buck, et al.

Pediatric Surgery International|June 16, 2019

Guidelines for the management of postoperative soiling in children with Hirschsprung diseaseP Saadai, A F Trappey, A M Goldstein, et al.

Carcinogenesis|November 4, 2000

High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern ChinaJ Huang, N Hu, A M Goldstein, et al.

Human Mutation|May 29, 1998

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutationsP M Pollock, N Spurr, T Bishop, et al.

Genes, Chromosomes & Cancer|July 4, 2001

Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinomaG Li, N Hu, A M Goldstein, et al.

The British Journal of Dermatology|December 3, 2020

Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneityR Laskar, A Ferreiro-Iglesias, D T Bishop, et al.

Anticancer Research|April 27, 1999

Familial and sporadic cases of nasopharyngeal carcinoma in TaiwanA Ung, C J Chen, P H Levine, et al.

Journal of Medical Genetics|June 7, 2005

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanomaK Laud, C Marian, M F Avril, et al.

Genes, Chromosomes & Cancer|February 19, 2000

Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese populationN Hu, M J Roth, M Polymeropolous, et al.

Pageof 15