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