Works matching IS 00099163 AND DT 2006 AND VI 69 AND IP 1

Results: 15

Genetic counseling for mental illness: goals resemble counseling goals for other common conditions.

Published in:

2006

By:

Biesecker, B. B.

Publication type:

Letter

CD36 expression and its relationship with obesity in blood cells from people with and without Prader-Willi syndrome.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 26, doi. 10.1111/j.1399-0004.2006.00536.x

By:

Webb, T.;
Whittington, J.;
A. J. Holland;
Soni, S.;
Boer, H.;
Clarke, D.;
Horsthemk, B.

Publication type:

Article

Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 86, doi. 10.1111/j.1399-0004.2006.00552.x

By:

Verdyck, P.;
Blaumeiser, B.;
Holder-Espinasse, M.;
Van Hul, W.;
W. Wuyts

Publication type:

Article

Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 21, doi. 10.1111/j.1399-0004.2006.00543a.x

By:

Lopez-Rangel, E.;
Lewis, M. E. S.

Publication type:

Article

Commentary on Duncan and Delatycki, 'Predictive genetic testing in young people for adult onset conditions: where is the empiric evidence?

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 17, doi. 10.1111/j.1399-0004.2006.00556.x

By:

Clarke, A.

Publication type:

Article

Authors' response to 'Genetic counseling for mental illness: goals not unlike counseling goals for other common conditions' by Barbara Bowles Biesecker.

Published in:

2006

By:

Austin, J. C.;
Honer, W. G.

Publication type:

Letter

Predictive genetic testing in young people for adult-onset conditions: Where is the empirical evidence?

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 8

By:

Duncana, R. E.;
Delatycki, M. B.

Publication type:

Article

Maternal urinary steroid profiles in prenatal diagnosis of Smith-Lemli-Opitz syndrome: first patient series comparing biochemical and molecular studies.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 77, doi. 10.1111/j.1399-0004.2006.00551.x

By:

Jezela-Stanek, A.;
Maunowicz, E. M.;
Ciara, E.;
Popowska, E.;
Goryluk-Kozakiewicz, B.;
Spodar, K.;
Czerwiecka, M.;
Jezuita, J.;
Nowaczyk, M. J. M.;
Krajewska-Walasek, M.

Publication type:

Article

Genetic and biochemical approach to early prenatal diagnosis in a family with mut methylmalonic aciduria.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 72, doi. 10.1111/j.1399-0004.2005.00547.x

By:

Cavicchi, C.;
Donati, M. A.;
Funghini, S.;
la Marca, G.;
Malvagia, S.;
Ciani, F.;
Poggi, G. M.;
Pasquini, E.;
Zammarchi, E.;
Morrone, A.

Publication type:

Article

Detection of human chromosomal abnormalities using a new technique combining 4',6-diamidino-2-phenyl-indole staining and image analysis.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 65, doi. 10.1111/j.1399-0004.2005.00544.x

By:

Liu, J. Y.;
Ji, M. F.;
Wang, X. R.;
Luo, R. L.;
Ren, X.;
Liu, M.;
Wang, Q. K.

Publication type:

Article

Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 58, doi. 10.1111/j.1399-0004.2005.00545.x

By:

Rooms, L.;
Reyniers, E.;
Wuyts, W.;
Storm, K.;
van Luijk, R.;
Scheers, S.;
Wauters, J.;
van den Ende, J.;
Biervliet, M.;
Eyskens, F.;
van Goethem, G.;
Laridon, A.;
Ceulemans, B.;
Courtens, W.;
Kooy, R. F.

Publication type:

Article

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening Study.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 48, doi. 10.1111/j.1399-0004.2006.00553.x

By:

Barton, J. C.;
Acton, R. T.;
Lovato, L.;
Speechley, M. R.;
McLaren, C. E.;
Harris, E. L.;
Reboussin, D. M.;
Adams, P. C.;
Dawkins, F. W.;
Gordeuk, V. R.;
Walker, A. P.

Publication type:

Article

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study).

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 40, doi. 10.1111/j.1399-0004.2006.00550.x

By:

Kurzawski, G.;
Suchy, J.;
Lener, M.;
Kłujszo-Grabowska, E.;
Kładny, J.;
Safranow, K.;
Jakubowska, K.;
Jakubowska, A.;
Huzarski, T.;
Byrski, T.;
Dȩbniak, T.;
Cybulski, C.;
Gronwald, J.;
Oszurek, O.;
Oszutowska, D.;
Kowalska, E.;
Góźdź, S.;
Niepsuj, S;
Słomski, R;
Pławski, A.

Publication type:

Article

Functional variants of the lipoprotein lipase gene and the risk of preeclampsia among non-Hispanic Caucasian women.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 33, doi. 10.1111/j.1399-0004.2005.00541.x

By:

Zhang, C.;
Austin, M. A.;
Edwards, K. L.;
Farin, F. M.;
Li, N.;
Hsu, L.;
Srinouanprachanh, S. L.;
Williams, M. A.

Publication type:

Article

Altered gene silencing and human diseases.

Published in:

Clinical Genetics, 2006, v. 69, n. 1, p. 1, doi. 10.1111/j.1399-0004.2005.00540.x

By:

Perini, G.;
Tupler, R.

Publication type:

Article