Works matching IS 14345161 AND DT 2002 AND VI 47 AND IP 3

Results: 7

Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 103, doi. 10.1007/s100380200010
By:
- Hilton, M. J.;
- Sawyer, J. M.;
- Gutiérrez, L.;
- Hogart, A.;
- Kung, T. C.;
- Wells, D. E.
Publication type:
Article
Impaired interactions between mouse Eya1 harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 107, doi. 10.1007/s100380200011
By:
- Ozaki, H.;
- Watanabe, Y.;
- Ikeda, K.;
- Kawakami, K.
Publication type:
Article
Anthropological implication of the SDF1-3′A allele distribution in Southeast Asia and Melanesia.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 117, doi. 10.1007/s100380200012
By:
- Kimura, R.;
- Soemantri, A.;
- Settheetham-Ishida, W.;
- Ohtsuka, R.;
- Inaoka, T.;
- Pookajorn, S.;
- Tiwawech, D.;
- Duanchang, P.;
- Ishida, T.
Publication type:
Article
Evidence for the de novo regeneration of the pattern of the length heteroplasmy associated with the T16189C variant in the control (D-loop) region of mitochondrial DNA.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 122, doi. 10.1007/s100380200013
By:
- Malik, S.;
- Sudoyo, H.;
- Pramoonjago, P.;
- Sukarna, T.;
- Darwis, D.;
- Marzuki, S.
Publication type:
Article
Association analysis of nine missense polymorphisms in the coagulation factor V gene with severe preeclampsia in pregnant Japanese women.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 131, doi. 10.1007/s100380200014
By:
- Watanabe, H.;
- Hamada, H.;
- Yamada, N.;
- Sohda, S.;
- Yamakawa-Kobayashi, K.;
- Yoshikawa, H.;
- Arinami, T.
Publication type:
Article
A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 136, doi. 10.1007/s100380200015
By:
- Kondoh, S.;
- Sugawara, H.;
- Harada, N.;
- Matsumoto, N.;
- Ohashi, H.;
- Sato, M.;
- Kantaputra, P. N.;
- Ogino, T.;
- Tomita, H.;
- Ohta, T.;
- Kishino, T.;
- Fukushima, Y.;
- Niikawa, N.;
- Yoshiura, K.
Publication type:
Article
Ethnic divergence and linkage disequilibrium of novel SNPs in the human NLI-IF gene: evidence of human origin and lack of association with tuberculosis susceptibility.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 3, p. 140, doi. 10.1007/s100380200016
By:
- Ma, X.;
- Wright, J.;
- Dou, S.;
- Olsen, P.;
- Teeter, L.;
- Adams, G.;
- Graviss, E.
Publication type:
Article

Works matching IS 14345161 AND DT 2002 AND VI 47 AND IP 3

Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes.

Impaired interactions between mouse Eya1 harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins.

Anthropological implication of the SDF1-3′A allele distribution in Southeast Asia and Melanesia.

Evidence for the de novo regeneration of the pattern of the length heteroplasmy associated with the T16189C variant in the control (D-loop) region of mitochondrial DNA.

Association analysis of nine missense polymorphisms in the coagulation factor V gene with severe preeclampsia in pregnant Japanese women.

A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet.

Ethnic divergence and linkage disequilibrium of novel SNPs in the human NLI-IF gene: evidence of human origin and lack of association with tuberculosis susceptibility.