Works matching IS 14345161 AND DT 2004 AND VI 49 AND IP 4

Results: 9

Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 177, doi. 10.1007/s10038-004-0128-5

By:

Kondo, Yuko;
Tsukishiro, Sami;
Tanemura, Mitsuyo;
Sugiura-Ogasawara, Mayumi;
Suzumori, Kaoru;
Sonta, Shin-ichi

Publication type:

Article

Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 187, doi. 10.1007/s10038-004-0131-x

By:

Tajima, Atsushi;
Hayami, Masanori;
Tokunaga, Katsushi;
Juji, Takeo;
Matsuo, Masafumi;
Marzuki, Sangkot;
Omoto, Keiichi;
Horai, Satoshi

Publication type:

Article

Evolutionary implication of human endogenous retrovirus HERV-H family.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 215, doi. 10.1007/s10038-004-0132-9

By:

Joo-Mi Yi;
Heui-Soo Kim

Publication type:

Article

Screening for point mutations in the LDL receptor gene in Bulgarian patients with severe hypercholesterolemia.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 173, doi. 10.1007/s10038-004-0127-6

By:

Mihaylov, Vassil A.;
Horvath, Anelia D.;
Savov, Alexey S.;
Kurshelova, Elina F.;
Paskaleva, Ivanka D.;
Goudev, Assen R.;
Stoilov, Ivaylo R.;
Ganev, Varban S.

Publication type:

Article

Identification of human Clock gene variants by denaturing high-performance liquid chromatography.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 209, doi. 10.1007/s10038-004-0130-y

By:

Ying Chen;
Ene-Choo Tan

Publication type:

Article

A novel alteration in metaxin 1, F202L, is associated with N370S in Gaucher disease.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 220, doi. 10.1007/s10038-004-0134-7

By:

LaMarca, Mary E.;
Goldstein, Mona;
Tayebi, Nahid;
Arcos-Burgos, Mauricio;
Martin, Brian M.;
Sidransky, Ellen

Publication type:

Article

Catalog of 300 SNPs in 23 genes encoding G-protein coupled receptors.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 194, doi. 10.1007/s10038-004-0133-8

By:

Iida, Aritoshi;
Saito, Susumu;
Sekine, Akihiro;
Kataoka, Yukie;
Tabei, Wataru;
Nakamura, Yusuke

Publication type:

Article

A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 182, doi. 10.1007/s10038-004-0129-4

By:

Kobashi, Gen;
Hata, Akira;
Ohta, Kaori;
Yamada, Hideto;
Kato, Emi Hirayama;
Minakami, Hisanori;
Fujimoto, Selichiro;
Kondo, Kiyotaro

Publication type:

Article

Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 4, p. 223, doi. 10.1007/s10038-004-0135-6

By:

Tate, Genshu;
Suzuki, Takao;
Kishimoto, Koji;
Mitsuya, Toshiyuki

Publication type:

Article