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M Shohat

Showing results (141-150 of 190) with videos related to

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Clinical Genetics|May 3, 2006
Expanding the phenotypic spectrum of L1CAM-associated diseaseL Basel-Vanagaite, R Straussberg, M J Friez, et al.
The British Journal of Dermatology|August 23, 2008
A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basisH N Baris, A Zlotogorski, G Peretz-Amit, et al.
American Journal of Medical Genetics|October 6, 1999
High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli AshkenazimT Sobe, P Erlich, A Berry, et al.
American Journal of Medical Genetics|October 1, 1989
Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequencyD B Rogers, M Shohat, G M Petersen, et al.
Journal of Assisted Reproduction and Genetics|July 4, 2001
Triple-test screening in in vitro fertilization pregnanciesI Bar-Hava, M Yitzhak, H Krissi, et al.
Journal of Medical Genetics|February 1, 1992
Sensorineural deafness inherited as a tissue specific mitochondrial disorderL Jaber, M Shohat, X Bu, et al.
British Journal of Cancer|July 17, 2003
Overexpression of a set of genes, including WISP-1, common to pulmonary metastases of both mouse D122 Lewis lung carcinoma and B16-F10.9 melanoma cell linesO Margalit, L Eisenbach, N Amariglio, et al.
American Journal of Medical Genetics|July 15, 1992
Late-onset localized junctional epidermolysis bullosa and mental retardation: a distinct autosomal recessive syndromeS Nakar, A Ingber, I Kremer, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 1, 1996
Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosidesI Braverman, L Jaber, H Levi, et al.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
Pageof 19

Showing results (141-150 of 190) with videos related to

Sort By:
Pageof 19
Clinical Genetics|May 3, 2006
Expanding the phenotypic spectrum of L1CAM-associated diseaseL Basel-Vanagaite, R Straussberg, M J Friez, et al.
The British Journal of Dermatology|August 23, 2008
A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basisH N Baris, A Zlotogorski, G Peretz-Amit, et al.
American Journal of Medical Genetics|October 6, 1999
High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli AshkenazimT Sobe, P Erlich, A Berry, et al.
American Journal of Medical Genetics|October 1, 1989
Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequencyD B Rogers, M Shohat, G M Petersen, et al.
Journal of Assisted Reproduction and Genetics|July 4, 2001
Triple-test screening in in vitro fertilization pregnanciesI Bar-Hava, M Yitzhak, H Krissi, et al.
Journal of Medical Genetics|February 1, 1992
Sensorineural deafness inherited as a tissue specific mitochondrial disorderL Jaber, M Shohat, X Bu, et al.
British Journal of Cancer|July 17, 2003
Overexpression of a set of genes, including WISP-1, common to pulmonary metastases of both mouse D122 Lewis lung carcinoma and B16-F10.9 melanoma cell linesO Margalit, L Eisenbach, N Amariglio, et al.
American Journal of Medical Genetics|July 15, 1992
Late-onset localized junctional epidermolysis bullosa and mental retardation: a distinct autosomal recessive syndromeS Nakar, A Ingber, I Kremer, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 1, 1996
Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosidesI Braverman, L Jaber, H Levi, et al.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
Pageof 19