Works matching IS 00099163 AND DT 1997 AND VI 51 AND IP 1

Results: 19

An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 61, doi. 10.1111/j.1399-0004.1997.tb02417.x

By:

Dundar, Munis;
Demiryilmaz, Fatma;
Demiryilmaz, Ilhan;
Kumandas, Sefer;
Erkilic, Kuddusi;
Kendirci, Mustafa;
Tuncel, Mehmet;
Ozyazgan, Isilay;
Tolmie, John L

Publication type:

Article

Spectrum of CFTR mutations in Argentine cystic fibrosis patients.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 43, doi. 10.1111/j.1399-0004.1997.tb02413.x

By:

Chertkoff, Lilien;
Visich, Alejandra;
Bienvenu, Thierry;
Grenoville, Mario;
Segal, Edgardo;
Carniglia, Luis;
Kaplan, Jean Claude;
Barreiro, Cristina

Publication type:

Article

Short Report on DNA Marker at Candidate Locus.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 76, doi. 10.1111/j.1399-0004.1997.tb02422.x

By:

Le, F.;
Zeng, X. P.;
Richelson, E.

Publication type:

Article

Association of angiotensin II type 1 receptor gene polymorphism with essential hypertension.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 31, doi. 10.1111/j.1399-0004.1997.tb02410.x

By:

Wang, William Y. S.;
Zee, Robert L;
Morris, Brian J.

Publication type:

Article

Interaction of the cholesteryl ester transfer protein I405V polymorphism with alcohol consumption in smoking and non-smoking healthy men, and the effect on plasma HDL cholesterol and apoAI concentration.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 15, doi. 10.1111/j.1399-0004.1997.tb02407.x

By:

Gudnason, V.;
Thormar, K.;
Humphries, S. E.

Publication type:

Article

Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 7, doi. 10.1111/j.1399-0004.1997.tb02406.x

By:

Mitchell, Simon;
Bundey, Sarah

Publication type:

Article

Association analysis of CA repeat polymorphism of the endothelial nitric oxide synthase gene with essential hypertension in Japanese.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 26, doi. 10.1111/j.1399-0004.1997.tb02409.x

By:

Nakayama, T.;
Soma, M.;
Takahashi, Y.;
Izumi, Y.;
Kanmatsuse, K.;
Esumi, M.

Publication type:

Article

Two mosaic-YY males carrying asymmetric Y chromosomes.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 65, doi. 10.1111/j.1399-0004.1997.tb02418.x

By:

Zelante, L.;
Dallapiccola, B.;
Calvano, S.;
Memeo, E.;
Gasparini, P.;
Simi, P.;
Rossi, S.;
Finelli, P.;
Rocchi, M.;
Archidiacono, N.

Publication type:

Article

Paracentric inversion of chromosome 9 with schizoaffective disorder.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 69, doi. 10.1111/j.1399-0004.1997.tb02419.x

By:

Inayama, Yasuhiro;
Yoneda, Hiroshi;
Fukushima, Kentaro;
Sakai, Jun;
Asaba, Hiroyuki;
Sakai, Toshiaki

Publication type:

Article

Chromosome deletion 17pl 1.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 71, doi. 10.1111/j.1399-0004.1997.tb02420.x

By:

Behjati, F.;
Mullarkey, M.;
Bergbaum, A.;
Berry, A. C.;
Docherty, Z.

Publication type:

Article

Genetic variation of the angiotensin-converting enzyme gene: increased frequency of the insertion allele in Koreans.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 35, doi. 10.1111/j.1399-0004.1997.tb02411.x

By:

Hong, S. H.;
Kang, B. Y.;
Park, W. H.;
Kim, J. Q.;
Lee, C. C.

Publication type:

Article

Short Report on DNA Marker at Candidate Locus.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 75, doi. 10.1111/j.1399-0004.1997.tb02421.x

By:

Kawanishi, Chiaki;
Osaka, Hitoshi;
Inoue, Ken;
Onishi, Hideki;
Yamada, Yoshiteru;
Kosaka, Kenji

Publication type:

Article

Are common mutations of cystathionine β-synthase involved in the aetiology of neural tube defects?

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 39, doi. 10.1111/j.1399-0004.1997.tb02412.x

By:

Ramsbottom, D.;
Scott, J.M.;
Molloy, A.;
Weir, D. G.;
Kirke, P. N.;
Mills, J. L.;
Gallagher, P. M.;
Whitehead, A. S.

Publication type:

Article

'Reduction' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 1, doi. 10.1111/j.1399-0004.1997.tb02405.x

By:

Loesch, Danuta Z.;
Petrovic, Vida;
Francis, David I.;
Oertel, Ralph;
Slater, Howard

Publication type:

Article

Oculopharyngeal muscular dystrophy (OPMD)-report and genetic studies of an Australian kindred.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 52, doi. 10.1111/j.1399-0004.1997.tb02415.x

By:

Teh, Bin Tean;
Sullivan, Alice-Ann;
Farnebo, Filip;
Zander, Cecilia;
Li, Fang Yuan;
Strachan, Noela;
Schalling, Martin;
Larsson, Catharina;
Sandstrom, Paul

Publication type:

Article

De novo duplication of 7pter→p21.2 and deletion of 9pter→p23.5: clinical and cytogenetic diagnosis.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 56, doi. 10.1111/j.1399-0004.1997.tb02416.x

By:

Back, E.;
Jung, C.;
Zeitler, S.;
Schempp, W.

Publication type:

Article

Short Report on DNA Marker at Candidate Locus.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 78, doi. 10.1111/j.1399-0004.1997.tb02423.x

By:

Guipponi, Michel;
Baldy-Moulinier, Michel;
Malafosse, Alain

Publication type:

Article

The role of the apolipoprotein E polymorphism in the prediction of coronary artery disease age of onset.

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 22, doi. 10.1111/j.1399-0004.1997.tb02408.x

By:

Moore, Jason H.;
Reilly, Sharon L;
Ferrell, Robert E.;
Sing, Charles F.

Publication type:

Article

Interstitial deletion of long arm of chromosome no. 5 with growth hormone deficiency-an emerging syndrome?

Published in:

Clinical Genetics, 1997, v. 51, n. 1, p. 48, doi. 10.1111/j.1399-0004.1997.tb02414.x

By:

Krishna, Jyoti;
Myers, Terry L;
Bourgeois, Michael J.;
Tonk, Vijay

Publication type:

Article