Works matching IS 14345161 AND DT 1999 AND VI 44 AND IP 1

Results: 18

Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 1, doi. 10.1007/s100380050096

By:

Miura, Kiyonori;
Miyoshi, Osamu;
Yun, Kankatsu;
Inazawa, Johji;
Miyamoto, Toshinobu;
Hayashi, H.;
Masuzaki, H.;
Yoshimura, Shuichiro;
Niikawa, Norio;
Jinno, Y.;
Ishimaru, Tadayuki

Publication type:

Article

Genome-wide scanning for type 2 diabetes susceptibility in Canadian Oji-Cree, using 190 microsatellite markers.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 10, doi. 10.1007/s100380050097

By:

Hegele, R. A.;
Sun, Fang;
Harris, Stewart B.;
Anderson, Carol;
Hanley, Anthony J. G.;
Zinman, Bernard

Publication type:

Article

Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 15, doi. 10.1007/s100380050098

By:

Murakami, Fumiyo;
Shimomura, T.;
Kotani, Kazuhiko;
Ikawa, Shiro;
Nanba, Eiji;
Adachi, Kaori

Publication type:

Article

Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 18, doi. 10.1007/s100380050099

By:

Shin, Ki-Hyuk;
Ku, J.-L.;
Park, J.-G.

Publication type:

Article

Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 22, doi. 10.1007/s100380050100

By:

Akaba, Kazuhiro;
Kimura, Toshiyuki;
Sasaki, Ayako;
Tanabe, Saori;
Wakabayashi, Takashi;
Hiroi, Masahiko;
Yasumura, Seiji;
Maki, Kazuko;
Aikawa, Shogo;
Hayasaka, K.

Publication type:

Article

Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 26, doi. 10.1007/s100380050101

By:

Miyake, H.;
Nagashima, Kanji;
Onigata, Kazumichi;
Nagashima, Tomohisa;
Takano, Yoko;
Morikawa, Akihiro

Publication type:

Article

Prevalence of congenital malformations and genetic diseases in Korea.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 30, doi. 10.1007/s100380050102

By:

Jung, S.-C.;
Kim, Sung-Soo;
Yoon, Kyung-Sik;
Lee, Jin-Sung

Publication type:

Article

Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut[sup 0] patients.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 35, doi. 10.1007/s100380050103

By:

Mikami, Hitoshi;
Ogasawara, Masahito;
Matsubara, Y.;
Kikuchi, Masahiro;
Miyabayashi, Shigeaki;
Kure, Shigeo;
Narisawa, Kuniaki

Publication type:

Article

No latent chromosome damage in oxygen-exposed premature neonates.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 40

By:

Méhes, Károly;
Bajnóczky, Katalin;
Adamovich, Károly;
Khezri, Seddiq;
Kosztolányi, György

Publication type:

Article

Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 43, doi. 10.1007/s100380050105

By:

Hamaguchi, K.;
Cong, Nguyen Duc;
Yanase, Toshihiko;
Ikuyama, Shoichiro;
Goto, Kiminobu;
Takayanagi, Ryoichi;
Nawata, Hajime;
Kusuda, Yoichiro;
Fukagawa, Koji;
Sakata, Toshiie

Publication type:

Article

Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 48, doi. 10.1007/s100380050106

By:

Nakamura, Asako;
Matsuura, Shinya;
Tauchi, Hiroshi;
Hanada, Ryoji;
Ohashi, Hirofumi;
Hasegawa, Tomonobu;
Honda, Koujiro;
Masuno, Mitsuo;
Imaizumi, Kiyoshi;
Sugita, Katsuo;
Ide, Toshinori;
Komatsu, K.

Publication type:

Article

Another observation of microphthalmia in an XX male: microphthalmia with linear skin defects syndrome without linear skin lesions.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 63, doi. 10.1007/s100380050110

By:

Kono, T.;
Migita, Takuo;
Koyama, Satomi;
Seki, Ichiro

Publication type:

Article

Localization of human midisatellite and macrosatellite DNA sequences on chromosomes 1 and X in the great apes.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 57, doi. 10.1007/s100380050108

By:

Samonte, Rhea V.;
Conte, Robert A.;
Verma, R. S.

Publication type:

Article

Autosomal dominant onychodystrophy and congenital sensorineural deafness.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 60, doi. 10.1007/s100380050109

By:

Kondoh, T.;
Tsuru, Akira;
Matsumoto, Tadashi;
Matsuzaka, Tetsuo;
Tsuji, Yoshiro

Publication type:

Article

Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1, showing homology to a metastasis-associated gene, MTA1.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 52, doi. 10.1007/s100380050107

By:

Futamura, Manabu;
Nishimori, Hiroyuki;
Shiratsuchi, Takayuki;
Saji, Shigetoyo;
Nakamura, Yusuke;
Tokino, T.

Publication type:

Article

A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 76, doi. 10.1007/s100380050113

By:

Mangino, Massimo;
Torrente, Isabella;
De Luca, Alessandro;
Sanchez, Otto;
Dallapiccola, Bruno;
Novelli, Giuseppe

Publication type:

Article

First case of missense mutation (LDH-H:R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patient.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 69, doi. 10.1007/s100380050111

By:

Hidaka, K.;
Ueda, Naoki;
Hirata, Ikuo;
Watanabe, Yoko;
Minatogawa, Yosuke;
Iuchi, Iwao

Publication type:

Article

Chromosomal mapping of two RBP-J-related genes: Kyo-T and RBP-L.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 1, p. 73, doi. 10.1007/s100380050112

By:

Tani, Shoichi;
Taniwaki, Masafumi;
Taniguchi, Yoshihito;
Minoguchi, Shigeru;
Kuroda, Kazuki;
Han, H.;
Aoki, Tomokazu;
Miyatake, Shin-ichi;
Hashimoto, Nobuo;
Honjo, T.

Publication type:

Article