Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 9

Results: 15

Rubinstein–Taybi syndrome.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 981, doi. 10.1038/sj.ejhg.5201594

By:

Hennekam, Raoul C M

Publication type:

Article

Rapid genotyping of common deficient thiopurine S-methyltransferase alleles using the DNA-microchip technique.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 991, doi. 10.1038/sj.ejhg.5201647

By:

Nasedkina, Tatyana V;
Fedorova, Olga E;
Glotov, Andrei S;
Chupova, Natalia V;
Samochatova, Elena V;
Maiorova, Olga A;
Zemlyakova, Valeria V;
Roudneva, Anastasia E;
Chudinov, Alexander V;
Yurasov, Roman A;
Kozhekbaeva, Janna M;
Barsky, Victor E;
Krynetskiy, Eugene Y;
Krynetskaia, Natalia F;
Cheng, Cheng;
Ribeiro, Raul C;
Evans, William E;
Roumyantsev, Alexander G;
Zasedatelev, Alexander S

Publication type:

Article

Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1018, doi. 10.1038/sj.ejhg.5201650

By:

Doan, Betty Q;
Sorant, Alexa J M;
Frangakis, Constantine E;
Bailey-Wilson, Joan E;
Shugart, Yin Y

Publication type:

Article

Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1–15q26.2.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 999, doi. 10.1038/sj.ejhg.5201652

By:

Slavotinek, Anne M.;
Moshrefi, Ali;
Davis, Randy;
Leeth, Elizabeth;
Schaeffer, G. Bradley;
Burchard, González Esteban;
Shaw, Gary M.;
James, Bristow;
Ptacek, Louis;
Pennacchio, Len A.

Publication type:

Article

Skin Cancer: Basal cell carcinoma: genetic homogeneity in a tumour type displaying phenotypic diversity.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 977, doi. 10.1038/sj.ejhg.5201658

By:

Hoban, Paul R.;
Lear, John T.;
Strange, Richard C.

Publication type:

Article

Pigmentary Diversity: Identifying the genes causing human diversity.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 978, doi. 10.1038/sj.ejhg.5201659

By:

Jackson, Ian J.

Publication type:

Article

Segregation ratio in cranio-cerebello-cardiac syndrome.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1054, doi. 10.1038/sj.ejhg.5201660

By:

Stellingwerff, Harm-Jan;
van Hagen, Johanna M.;
ten Kate, Leo P.

Publication type:

Article

Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1009, doi. 10.1038/sj.ejhg.5201661

By:

Saugier-Veber, Pascale;
Goldenberg, Alice;
Drouin-Garraud, Valérie;
de La Rochebrochard, Céline;
Layet, Valérie;
Drouot, Nathalie;
Le Meur, Nathalie;
Gilbert-Du-ssardier, Brigitte;
Joly-Hélas, Géraldine;
Moirot, Hélène;
Rossi, Annick;
Tosi, Mario;
Frébourg, Thierry

Publication type:

Article

The population history of the Croatian linguistic minority of Molise (southern Italy): a maternal view.

Published in:

2006

By:

Babalini, Carla;
Martínez-Labarga, Cristina;
Tolk, Helle-Viivi;
Kivisild, Toomas;
Giampaolo, Rita;
Tarsi, Tiziana;
Contini, Irene;
Barać, Lovorka;
Janićijević, Branka;
Klarić, Irena Martinović;
Peričić, Marijana;
Sujoldžić, Anita;
Villems, Richard;
Biondi, Gianfranco;
Rudan, Pavao;
Rickards, Olga

Publication type:

Correction Notice

A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1037, doi. 10.1038/sj.ejhg.5201664

By:

Winantea, Jane;
Hoang, My Ngo;
Ohlraun, Stefanie;
Rietschel, Marcella;
Cichon, Sven;
Propping, Peter;
Nöthen, Markus M.;
Freudenberg, Jan;
Freudenberg-Hua, Yun

Publication type:

Article

2nd International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism.

Published in:

2006

By:

Romano, C.

Publication type:

Report

The effective size of the Icelandic population and the prospects for LD mapping: inference from unphased microsatellite markers.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1044, doi. 10.1038/sj.ejhg.5201669

By:

Bataillon, Thomas;
Mailund, Thomas;
Thorlacius, Steinunn;
Steingrimsson, Eirikur;
Rafnar, Thorunn;
Halldorsson, Magnus M.;
Calian, Violeta;
Schierup, Mikkel H.

Publication type:

Article

New mutations in the NHS gene in Nance–Horan Syndrome families from the Netherlands.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 986, doi. 10.1038/sj.ejhg.5201671

By:

Florijn, Ralph J.;
Loves, Willem;
Maillette de Buy Wenniger-Prick, Liesbeth J. J. M.;
Mannens, Marcel M. A. M.;
Tijmes, Nel;
Brooks, Simon P.;
Hardcastle, Alison J.;
Bergen, Arthur A. B.

Publication type:

Article

ADAM33 haplotypes are associated with asthma in a large Australian population.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1027, doi. 10.1038/sj.ejhg.5201662

By:

Kedda, Mary-Anne;
Duffy, David L.;
Bradley, Bernadette;
O'Hehir, Robyn E.;
Thompson, Philip J.

Publication type:

Article

Meta-analysis of TNF-α promoter −308 A/G polymorphism and SLE susceptibility.

Published in:

2006

By:

Lee, Young Ho;
Harley, John B.;
Nath, Swapan K.

Publication type:

Correction Notice