Works matching IS 10184813 AND DT 2001 AND VI 9 AND IP 10

Results: 14

DNA sequence variability of IGHG3 alleles associated to the main G3m haplotypes in human populations.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 765, doi. 10.1038/sj.ejhg.5200700

By:

Dard, Patricia;
Lefranc, Marie-Paule;
Osipova, Ludmilla;
Sanchez-Mazas, Alicia

Publication type:

Article

A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 753

By:

Børglum, Anders D;
Balslev, Thomas;
Haagerup, Annette;
Birkebæk, Niels;
Binderup, Helle;
Kruse, Torben A;
Hertz, Jens Michael

Publication type:

Article

Serum myeloperoxidase concentration in a healthy population: biological variations, familial resemblance and new genetic polymorphisms.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 780, doi. 10.1038/sj.ejhg.5200702

By:

Hoy, Aline;
Trégouët, David;
Leininger-Muller, Brigitte;
Poirier, Odette;
Maurice, Mickaël;
Sass, Catherine;
Siest, Gérard;
Tiret, Laurence;
Visvikis, Sophie

Publication type:

Article

The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 787, doi. 10.1038/sj.ejhg.5200704

By:

Bergman, Annika;
Einbeigi, Zakaria;
Olofsson, Ulrica;
Taib, Ziad;
Wallgren, Arne;
Karlsson, Per;
Wahlström, Jan;
Martinsson, Tommy;
Nordling, Margareta

Publication type:

Article

Absence of the HIV-1 protective Δccr5 allele in most ethnic populations of India.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 794, doi. 10.1038/sj.ejhg.5200705

By:

Majumder, Partha P;
Dey, Badal

Publication type:

Article

Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 731

By:

Zouali, Habib;
Chamaillard, Mathias;
Lesage, Suzane;
Cézard, Jean-Pierre;
Colombel, Jean-Frédéric;
Belaiche, Jacques;
Almer, Sven;
Tysk, Curt;
Montague, Sean;
Gassull, Miquel;
Christensen, Steen;
Finkel, Yigael;
Gower-Rousseau, Corine;
Modigliani, Robert;
Macry, Jeanne;
Selinger-Leneman, Hana;
Thomas, Gilles;
Hugot, Jean-Pierre

Publication type:

Article

A genome-wide scan for preeclampsia in the Netherlands.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 758, doi. 10.1038/sj.ejhg.5200706

By:

Lachmeijer, Augusta MA;
Arngrímsson, Reynir;
Bastiaans, Esther J;
Frigge, Michael L;
Pals, Gerald;
Sigurdardóttir, Sigrun;
Stéfansson, Hreinn;
Pálsson, Birgir;
Nicolae, Dan;
Kong, Augustin;
Aarnoudse, Jan G;
Gulcher, Jeff R;
Dekker, Guustaaf A;
ten Kate, Leo P;
Stéfansson, Kári

Publication type:

Article

The angiotensin converting enzyme I/D polymorphism in Russian athletes.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 797, doi. 10.1038/sj.ejhg.5200711

By:

Nazarov, Igor B;
Woods, David R;
Montgomery, Hugh E;
Shneider, Olga V;
Kazakov, Vasiliy I;
Tomilin, Nikolai V;
Rogozkin, Viktor A

Publication type:

Article

An mtDNA mutation, 14453G→A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 805, doi. 10.1038/sj.ejhg.5200712

By:

Ravn, Kirstine;
Wibrand, Flemming;
Hansen, Flemming Juul;
Horn, Nina;
Rosenberg, Thomas;
Schwartz, Marianne

Publication type:

Article

Investigations of a CA repeat in the oestrogen receptor β gene in patients with Alzheimer's disease.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 802, doi. 10.1038/sj.ejhg.5200714

By:

Forsell, Charlotte;
Enmark, Eva;
Axelman, Karin;
Blomberg, Mari;
Wahlund, Lars-Olof;
Gustafsson, Jan-Åke;
Lannfelt, Lars

Publication type:

Article

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 747, doi. 10.1038/sj.ejhg.5200713

By:

Koillinen, Hannele;
Wong, Fung Ki;
Rautio, Jorma;
Ollikainen, Vesa;
Karsten, Agneta;
Larson, Ola;
Teh, Bin Tean;
Huggare, Jan;
Lahermo, Päivi;
Larsson, Catharina;
Kere, Juha

Publication type:

Article

Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 773, doi. 10.1038/sj.ejhg.5200717

By:

Barkardottir, Rosa B;
Sarantaus, Laura;
Arason, Adalgeir;
Vehmanen, Paula;
Bendahl, Pär-Ola;
Kainu, Tommi;
Syrjäkoski, Kirsi;
Krahe, Ralf;
Huusko, Pia;
Pyrhönen, Seppo;
Holli, Kaija;
Kallioniemi, Olli-P;
Egilsson, Valgardur;
Kere, Juha;
Nevanlinna, Heli

Publication type:

Article

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 743, doi. 10.1038/sj.ejhg.5200715

By:

Nieminen, Pekka;
Arte, Sirpa;
Tanner, Dennis;
Paulin, Lars;
Alaluusua, Satu;
Thesleff, Irma;
Pirinen, Sinikka

Publication type:

Article

Medical genomics.

Published in:

2001

By:

van Ommen, Gert-Jan B

Publication type:

Editorial