Works matching IS 10184813 AND DT 2007 AND VI 15 AND IP 4

Results: 18

Ashkenazi Jewish mtDNA haplogroup distribution varies among distinct subpopulations: lessons of population substructure in a closed group.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 498, doi. 10.1038/sj.ejhg.5201764

By:

Feder, Jeanette;
Ovadia, Ofer;
Glaser, Benjamin;
Mishmar, Dan

Publication type:

Article

Most pooling variation in array-based DNA pooling is attributable to array error rather than pool construction error.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 501, doi. 10.1038/sj.ejhg.5201768

By:

Macgregor, Stuart

Publication type:

Article

FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 405, doi. 10.1038/sj.ejhg.5201777

By:

Beleza-Meireles, Ana;
Lundberg, Fredrik;
Lagerstedt, Kristina;
Zhou, Xiaolei;
Omrani, Davood;
Frisén, Louise;
Nordenskjöld, Agneta

Publication type:

Article

Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 411, doi. 10.1038/sj.ejhg.5201770

By:

Vendramini, Siulan;
Richieri-Costa, Antonio;
Guion-Almeida, Maria Leine

Publication type:

Article

The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutation.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 453, doi. 10.1038/sj.ejhg.5201774

By:

Decruyenaere, Marleen;
Evers-Kiebooms, Gerry;
Boogaerts, Andrea;
Philippe, Kristien;
Demyttenaere, Koen;
Dom, René;
Vandenberghe, Wim;
Fryns, Jean-Pierre

Publication type:

Article

Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 432, doi. 10.1038/sj.ejhg.5201775

By:

Mignon-Ravix, Cécile;
Depetris, Danielle;
Luciani, Judith J.;
Cuoco, Cristina;
Krajewska-Walasek, Malgorzata;
Missirian, Chantal;
Collignon, Patrick;
Delobel, Bruno;
Croquette, Marie-Françoise;
Moncla, Anne;
Kroisel, Peter M.;
Mattei, Marie-Geneviève

Publication type:

Article

Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange Syndrome.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 505, doi. 10.1038/sj.ejhg.5201776

By:

Bhuiyan, Zahurul A.;
Stewart, Helen;
Redeker, Egbert J.;
Mannens, Marcel M. A. M.;
Hennekam, Raoul C. M.

Publication type:

Article

Paleolithic Y-haplogroup heritage predominates in a Cretan highland plateau.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 485, doi. 10.1038/sj.ejhg.5201769

By:

Martinez, Laisel;
Underhill, Peter A.;
Zhivotovsky, Lev A.;
Gayden, Tenzin;
Moschonas, Nicholas K.;
Chow, Cheryl-Emiliane T.;
Conti, Simon;
Mamolini, Elisabetta;
Cavalli-Sforza, L. Luca;
Herrera, Rene J.

Publication type:

Article

CHARGE syndrome: an update.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 389, doi. 10.1038/sj.ejhg.5201778

By:

Sanlaville, Damien;
Verloes, Alain

Publication type:

Article

Distribution of the D15Z1 copy number polymorphism.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 441, doi. 10.1038/sj.ejhg.5201780

By:

Cockwell, Annette E.;
Jacobs, Patricia A.;
Crolla, John A.

Publication type:

Article

‘Distorted’ mitochondrial DNA sequences in schizophrenic patients.

Published in:

2007

By:

Bandelt, Hans-Jürgen;
Olivieri, Anna;
Bravi, Claudio;
Yao, Yong-Gang;
Torroni, Antonio;
Salas, Antonio

Publication type:

Letter

Reply to Bandelt et al.

Published in:

2007

By:

Martorell, Lourdes;
Vilella, Elisabet

Publication type:

Letter

Linkage and association analysis of CACNG3 in childhood absence epilepsy.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 463, doi. 10.1038/sj.ejhg.5201783

By:

Everett, Kate V.;
Chioza, Barry;
Aicardi, Jean;
Aschauer, Harald;
Brouwer, Oebele;
Callenbach, Petra;
Covanis, Athanasios;
Dulac, Olivier;
Eeg-Olofsson, Orvar;
Feucht, Martha;
Friis, Mogens;
Goutieres, Françoise;
Guerrini, Renzo;
Heils, Armin;
Kjeldsen, Marianne;
Lehesjoki, Anna-Elina;
Makoff, Andrew;
Nabbout, Rima;
Olsson, Ingrid;
Sander, Thomas

Publication type:

Article

Genotype–phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the ‘association des Cytogénéticiens de langue Française’.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 446, doi. 10.1038/sj.ejhg.5201784

By:

Béri-Deixheimer, Mylène;
Gregoire, Marie-José;
Toutain, Annick;
Brochet, Karène;
Briault, Sylvain;
Schaff, Jean-Luc;
Leheup, Bruno;
Jonveaux, Philippe

Publication type:

Article

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 422, doi. 10.1038/sj.ejhg.5201785

By:

Castermans, Dries;
Vermeesch, Joris R.;
Fryns, Jean-Pierre;
Steyaert, Jean G.;
Van de Ven, Wim J. M.;
Creemers, John W M;
Devriendt, Koen

Publication type:

Article

A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 473, doi. 10.1038/sj.ejhg.5201787

By:

Dehainault, Catherine;
Michaux, Dorothée;
Pagès-Berhouet, Sabine;
Caux-Moncoutier, Virginie;
Doz, François;
Desjardins, Laurence;
Couturier, Jérôme;
Parent, Philippe;
Stoppa-Lyonnet, Dominique;
Gauthier-Villars, Marion;
Houdayer, Claude

Publication type:

Article

Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 494, doi. 10.1038/sj.ejhg.5201788

By:

Kivinen, Katja;
Peterson, Hanna;
Hiltunen, Leena;
Laivuori, Hannele;
Heino, Sanna;
Tiala, Inkeri;
Knuutila, Sakari;
Rasi, Vesa;
Kere, Juha

Publication type:

Article

Angiotensinogen M235T polymorphism and the risk of myocardial infarction and stroke among hypertensive patients on ACE-inhibitors or β-blockers.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 478, doi. 10.1038/sj.ejhg.5201789

By:

Schelleman, Hedi;
Klungel, Olaf H.;
Witteman, Jacqueline C. M.;
Breteler, Monique M. B.;
Yazdanpanah, Moygan;
Danser, A. H. Jan;
Hofman, Albert;
van Duijn, Cornelia M.;
de Boer, Anthonius;
Stricker, Bruno H. Ch

Publication type:

Article