Works matching IS 10184813 AND DT 2003 AND VI 11 AND IP 8

Results: 14

Computer-based recognition of dysmorphic faces.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 555, doi. 10.1038/sj.ejhg.5200997

By:

Loos, Hartmut S;
Wieczorek, Dagmar;
Würtz, Rolf P;
Malsburg, Christoph von der;
Horsthemke, Bernhard

Publication type:

Article

Genetic information and life insurance: a ‘real’ risk?

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 561, doi. 10.1038/sj.ejhg.5200998

By:

Joly, Yann;
Knoppers, Bartha M;
Godard, Béatrice

Publication type:

Article

Manic depressive illness in a founder population.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 597, doi. 10.1038/sj.ejhg.5201001

By:

Heyer, Evelyne;
Toupance, Bruno;
Perri, Cesare;
De Vito, Ornella;
Foncin, Jean-François;
Cecilia Bruni, Amalia

Publication type:

Article

Comment on ‘CFTR gene mutations in sarcoidosis’.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 553, doi. 10.1038/sj.ejhg.5201003

By:

Bombieri, Cristina;
Belpinati, Francesca;
Pignatti, Pier Franco;
Luisetti, Maurizio

Publication type:

Article

A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 623, doi. 10.1038/sj.ejhg.5201005

By:

Rafique, Muhammad Arshad;
Ansar, Muhammad;
Jamal, Syed Muhammad;
Malik, Sajid;
Sohail, Muhammad;
Faiyaz-Ul-Haque, Mohammad;
Haque, Sayedul;
Leal, Suzanne M;
Ahmad, Wasim

Publication type:

Article

Medical and lay attitudes towards genetic screening and testing in Finland.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 565, doi. 10.1038/sj.ejhg.5201006

By:

Toiviainen, Hanna;
Jallinoja, Piia;
Aro, Arja R;
Hemminki, Elina

Publication type:

Article

Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 573, doi. 10.1038/sj.ejhg.5201008

By:

Böhringer, Stefan;
Hardt, Cornelia;
Miterski, Bianca;
Steland, Ansgar;
Epplen, Jörg T

Publication type:

Article

Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 585, doi. 10.1038/sj.ejhg.5201009

By:

Rivard, Sylvain R;
Lanzara, Carmela;
Grimard, Doria;
Carella, Massimo;
Simard, Hervey;
Ficarella, Romina;
Simard, Raynald;
D'Adamo, Adamo Pio;
Férec, Claude;
Camaschella, Clara;
Mura, Cathrine;
Roetto, Antonella;
De Braekeleer, Marc;
Bechner, Lucien;
Gasparini, Paolo

Publication type:

Article

Genetic variation at the human tissue-type plasminogen activator (tPA) locus: haplotypes and analysis of association to plasma levels of tPA.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 603, doi. 10.1038/sj.ejhg.5201011

By:

Ladenvall, P;
Nilsson, S;
Jood, K;
Rosengren, A;
Blomstrand, C;
Jern, C

Publication type:

Article

Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 611, doi. 10.1038/sj.ejhg.5201012

By:

Hauben, E I;
Arends, J;
Vandenbroucke, J P;
van Asperen, C J;
Van Marck, E;
Hogendoorn, P C W

Publication type:

Article

Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 590, doi. 10.1038/sj.ejhg.5201014

By:

Dizier, M-H;
Quesneville, H;
Besse-Schmittler, C;
Guilloud-Bataille, M;
Selinger-Leneman, H;
Clerget-Darpoux, F;
Demenais, F

Publication type:

Article

Promoter polymorphism influences the effect of dexamethasone on transcriptional activation of the LTC<sub>4</sub> synthase gene.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 619, doi. 10.1038/sj.ejhg.5201015

By:

Sayers, I;
Sampson, A P;
Ye, S;
Holgate, S T

Publication type:

Article

SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 629, doi. 10.1038/sj.ejhg.5201018

By:

Zühlke, C H;
Spranger, M;
Spranger, S;
Voigt, R;
Lanz, M;
Gehlken, U;
Hinrichs, F;
Schwinger, E

Publication type:

Article

Possible consequences of applying guidelines to healthy women with a family history of breast cancer.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 633, doi. 10.1038/sj.ejhg.5201021

By:

van Asperen, C J;
Tollenaar, R A E M;
Krol-Warmerdam, E M M;
Blom, J;
Hoogendoorn, W E;
Seynaeve, C M J C;
Brekelmans, C T M;
Devilee, P;
Cornelisse, C J;
Klijn, J G M;
de Bock, G H

Publication type:

Article