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Annals of Neurology|May 1, 1997

Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.

Neurology|March 1, 1995

A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.

Medical and Pediatric Oncology|April 1, 1996

Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth diseaseY Neumann, A Toren, G Rechavi, et al.

Molecular Psychiatry|June 21, 2007

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish familiesT Venken, M Alaerts, D Souery, et al.

Journal of the Neurological Sciences|January 1, 1997

Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblingsE Hund, A Grau, W Fogel, et al.

American Journal of Human Genetics|October 1, 1992

A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.

Molecular Psychiatry|July 8, 1999

hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21V Dror, E Shamir, S Ghanshani, et al.

Oncogene|December 20, 2011

Deubiquitination of EGFR by Cezanne-1 contributes to cancer progressionF Pareja, D A Ferraro, C Rubin, et al.

Human Mutation|September 23, 1998

Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish populationM Horowitz, M Pasmanik-Chor, Z Borochowitz, et al.

European Journal of Human Genetics : EJHG|January 1, 1996

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative studyE Nelis, C Van Broeckhoven, P De Jonghe, et al.

Pageof 5

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

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 50 results.

Annals of Neurology|May 1, 1997

Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.

Neurology|March 1, 1995

A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.

Medical and Pediatric Oncology|April 1, 1996

Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth diseaseY Neumann, A Toren, G Rechavi, et al.

Molecular Psychiatry|June 21, 2007

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish familiesT Venken, M Alaerts, D Souery, et al.

Journal of the Neurological Sciences|January 1, 1997

Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblingsE Hund, A Grau, W Fogel, et al.

American Journal of Human Genetics|October 1, 1992

A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.

Molecular Psychiatry|July 8, 1999

hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21V Dror, E Shamir, S Ghanshani, et al.

Oncogene|December 20, 2011

Deubiquitination of EGFR by Cezanne-1 contributes to cancer progressionF Pareja, D A Ferraro, C Rubin, et al.

Human Mutation|September 23, 1998

Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish populationM Horowitz, M Pasmanik-Chor, Z Borochowitz, et al.

European Journal of Human Genetics : EJHG|January 1, 1996

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative studyE Nelis, C Van Broeckhoven, P De Jonghe, et al.

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