Works matching IS 03406717 AND DT 2002 AND VI 110 AND IP 2

Results: 14

ZNT4 gene is not responsible for acrodermatitis enteropathica in Japanese families.

Published in:: Human Genetics, 2002, v. 110, n. 2, p. 201, doi. 10.1007/s00439-001-0661-7
Publication type:: Article

Y-chromosomal evidence for a strong reduction in male population size of Yakuts.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 198, doi. 10.1007/s00439-001-0664-4

By:

Pakendorf, Brigitte;
Morar, Bharti;
Tarskaia, Larissa A.;
Kayser, Manfred;
Soodyall, Himla;
Rodewald, Alexander;
Stoneking, Mark

Publication type:

Article

Susceptibility gene for non-obstructive azoospermia located near HLA-DR and -DQ loci in the HLA class II region.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 192, doi. 10.1007/s00439-001-0657-3

By:

Tsujimura, Akira;
Ota, Masao;
Katsuyama, Yoshihiko;
Sada, Masaharu;
Miura, Hidenobu;
Matsumiya, Kiyomi;
Gotoh, Rieko;
Nakatani, Takeshi;
Okuyama, Akihiko;
Takahara, Shiro

Publication type:

Article

Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 145, doi. 10.1007/s00439-002-0680-z

By:

Ahlbom, Bodil;
Yaqoob, Muhammad;
Gustavsson, Peter;
Abbas, Hafez;
Annerén, Göran;
Larsson, Agne;
Wadelius, Claes

Publication type:

Article

Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 122, doi. 10.1007/s00439-001-0662-6

By:

Chang, Bao-li;
Zheng, Siqun L.;
Hawkins, Gregory A.;
Isaacs, Sarah D.;
Wiley, Kathy E.;
Turner, Aubrey;
Carpten, John D.;
Bleecker, Eugene R.;
Walsh, Patrick C.;
Trent, Jeffrey M.;
Meyers, Deborah A.;
Isaacs, William B.;
Xu, Jianfeng

Publication type:

Article

Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 173, doi. 10.1007/s00439-001-0663-5

By:

Gu, Dongfeng;
O'Dell, Sandra D.;
Chen, Xiao-he;
Miller, George J.;
Day, Ian N.

Publication type:

Article

Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitus.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 139, doi. 10.1007/s00439-001-0671-5

By:

Mackay, D.;
Coupe, A.-M.;
Shield, J.;
Storr, J.;
Temple, I.;
Robinson, D.

Publication type:

Article

Pyruvate dehydrogenase E3 binding protein deficiency.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 187, doi. 10.1007/s00439-001-0665-3

By:

Brown, Ruth M.;
Head, Rosie A.;
Brown, Garry K.

Publication type:

Article

Effectiveness of computational methods in haplotype prediction.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 148, doi. 10.1007/s00439-001-0656-4

By:

Xu, Chun-Fang;
Lewis, Karen;
Cantone, Kathryn L.;
Khan, Parveen;
Donnelly, Christine;
White, Nicola;
Crocker, Nikki;
Boyd, Pete R.;
Zaykin, Dmitri V.;
Purvis, Ian J.

Publication type:

Article

A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 111, doi. 10.1007/s00439-001-0646-6

By:

Rozenblum, Ester;
Vahteristo, Pia;
Sandberg, Therese;
Bergthorsson, Jon;
Syrjakoski, Kirsi;
Weaver, Don;
Haraldsson, Karin;
Johannsdottir, Hrefna;
Vehmanen, Paula;
Nigam, Savita;
Golberger, Natalie;
Robbins, Christiane;
Pak, Evgenia;
Dutra, Amalia;
Gillander, Elizabeth;
Stephan, Dietrich A.;
Bailey-Wilson, Joan;
Juo, Suh-Hang;
Kainu, Tommi;
Arason, Adalgeir

Publication type:

Article

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 182, doi. 10.1007/s00439-001-0659-1

By:

Seri, Marco;
Savino, Maria;
Bordo, Domenico;
Cusano, Roberto;
Rocca, Bianca;
Meloni, Ilaria;
Bari, Filomena;
Koivisto, Pasi A.;
Bolognesi, Martino;
Ghiggeri, Gian;
Landolfi, Raffaele;
Balduini, Carlo L.;
Zelante, Leopoldo;
Ravazzolo, Roberto;
Renieri, Alessandra;
Savoia, Anna

Publication type:

Article

Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 166, doi. 10.1007/s00439-001-0647-5

By:

Watts, Giles D.;
O'Briant, Kathy C.;
Chance, Phillip F.

Publication type:

Article

Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 157, doi. 10.1007/s00439-001-0655-5

By:

Schön, Patric;
Tsuchiya, Ken;
Lenoir, Didier;
Mochizuki, Toshio;
Guichard, Cécile;
Takai, Setsuo;
Maiti, Amit K.;
Nihei, Hiroshi;
Weil, Johan;
Yokoyama, Takahiko;
Bouvagnet, Patrice

Publication type:

Article

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

Published in:

Human Genetics, 2002, v. 110, n. 2, p. 130, doi. 10.1007/s00439-001-0660-8

By:

Brown, Michael D.;
Starikovskaya, Elena;
Derbeneva, Olga;
Hosseini, Seyed;
Allen, Jon C.;
Mikhailovskaya, Irina E.;
Sukernik, Rem I.;
Wallace, Douglas C.

Publication type:

Article