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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 5, 2001
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness
Y Bykhovskaya, H Yang, K Taylor, et al.
American Journal of Human Genetics
|
May 2, 2000
Candidate locus for a nuclear modifier gene for maternally inherited deafness
Y Bykhovskaya, X Estivill, K Taylor, et al.
American Journal of Human Genetics
|
May 1, 1997
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families
E Levy-Lahad, R Catane, S Eisenberg, et al.
Human Genetics
|
September 12, 2000
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population
T Sobe, S Vreugde, H Shahin, et al.
Dermatology (Basel, Switzerland)
|
January 21, 2000
Atopic dermatitis and HTLV-1-associated myelopathy: associated or coincidental disorders?
M Shohat, D Ben Amitai, B Shohat, et al.
American Journal of Medical Genetics
|
June 19, 1998
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation
Y Bykhovskaya, M Shohat, K Ehrenman, et al.
Clinical Genetics
|
June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel
G Borck, L Rainshtein, S Hellman-Aharony, et al.
American Journal of Medical Genetics
|
November 7, 1998
Correlation of linkage data with phenotype in eight families with Stickler syndrome
D J Wilkin, G R Mortier, C L Johnson, et al.
Pediatrics
|
May 9, 2000
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis
A Mimouni, N Magal, N Stoffman, et al.
American Journal of Medical Genetics
|
August 1, 1994
Desbuquois syndrome: clinical, radiographic, and morphologic characterization
M Shohat, R Lachman, H E Gruber, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 190) with videos related to
Sort By:
Page
of 19
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 5, 2001
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness
Y Bykhovskaya, H Yang, K Taylor, et al.
American Journal of Human Genetics
|
May 2, 2000
Candidate locus for a nuclear modifier gene for maternally inherited deafness
Y Bykhovskaya, X Estivill, K Taylor, et al.
American Journal of Human Genetics
|
May 1, 1997
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families
E Levy-Lahad, R Catane, S Eisenberg, et al.
Human Genetics
|
September 12, 2000
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population
T Sobe, S Vreugde, H Shahin, et al.
Dermatology (Basel, Switzerland)
|
January 21, 2000
Atopic dermatitis and HTLV-1-associated myelopathy: associated or coincidental disorders?
M Shohat, D Ben Amitai, B Shohat, et al.
American Journal of Medical Genetics
|
June 19, 1998
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation
Y Bykhovskaya, M Shohat, K Ehrenman, et al.
Clinical Genetics
|
June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel
G Borck, L Rainshtein, S Hellman-Aharony, et al.
American Journal of Medical Genetics
|
November 7, 1998
Correlation of linkage data with phenotype in eight families with Stickler syndrome
D J Wilkin, G R Mortier, C L Johnson, et al.
Pediatrics
|
May 9, 2000
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis
A Mimouni, N Magal, N Stoffman, et al.
American Journal of Medical Genetics
|
August 1, 1994
Desbuquois syndrome: clinical, radiographic, and morphologic characterization
M Shohat, R Lachman, H E Gruber, et al.
Page
of 19