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Progress in Clinical and Biological Research
|
January 1, 1993
Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1A
B B Roa, C A Garcia, C A Wise, et al.
Nucleic Acids Research
|
February 25, 1990
Isolation of a polymorphic DNA sequence (LL101) from the short arm of chromosome 17 [D17S251]
P I Patel, D H Ledbetter, S Frances, et al.
Archives of Oral Biology
|
July 26, 2008
Tooth dimensions in hypodontia with a known PAX9 mutation
A H Brook, C Elcock, M Aggarwal, et al.
Schizophrenia Research
|
January 1, 1993
Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia
A R Sanders, D E Rincon-Limas, R Chakraborty, et al.
Neurology
|
August 26, 1998
Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy
F Zara, M Labuda, P G Garofalo, et al.
American Journal of Human Genetics
|
May 1, 1997
Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions
S P Yang, S I Bidichandani, L E Figuera, et al.
Clinical Genetics
|
June 2, 2007
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases
E A Edelman, S Girirajan, B Finucane, et al.
American Journal of Medical Genetics
|
December 10, 1999
Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndrome
S H Elsea, K Mykytyn, K Ferrell, et al.
American Journal of Human Genetics
|
April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17
P I Patel, B Franco, C Garcia, et al.
American Journal of Human Genetics
|
June 1, 1994
Detection of tandem duplications and implications for linkage analysis
T C Matise, A Chakravarti, P I Patel, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 85) with videos related to
Sort By:
Page
of 9
Progress in Clinical and Biological Research
|
January 1, 1993
Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1A
B B Roa, C A Garcia, C A Wise, et al.
Nucleic Acids Research
|
February 25, 1990
Isolation of a polymorphic DNA sequence (LL101) from the short arm of chromosome 17 [D17S251]
P I Patel, D H Ledbetter, S Frances, et al.
Archives of Oral Biology
|
July 26, 2008
Tooth dimensions in hypodontia with a known PAX9 mutation
A H Brook, C Elcock, M Aggarwal, et al.
Schizophrenia Research
|
January 1, 1993
Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia
A R Sanders, D E Rincon-Limas, R Chakraborty, et al.
Neurology
|
August 26, 1998
Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy
F Zara, M Labuda, P G Garofalo, et al.
American Journal of Human Genetics
|
May 1, 1997
Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions
S P Yang, S I Bidichandani, L E Figuera, et al.
Clinical Genetics
|
June 2, 2007
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases
E A Edelman, S Girirajan, B Finucane, et al.
American Journal of Medical Genetics
|
December 10, 1999
Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndrome
S H Elsea, K Mykytyn, K Ferrell, et al.
American Journal of Human Genetics
|
April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17
P I Patel, B Franco, C Garcia, et al.
American Journal of Human Genetics
|
June 1, 1994
Detection of tandem duplications and implications for linkage analysis
T C Matise, A Chakravarti, P I Patel, et al.
Page
of 9