Works matching IS 00099163 AND DT 1999 AND VI 55 AND IP 6

Results: 20

Recombinant proteins for genetic disease.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 389, doi. 10.1034/j.1399-0004.1999.550601.x

By:

Russell, Chris S.;
Clarke, Lorne A.

Publication type:

Article

HotSpots: The Fat gene.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 395, doi. 10.1034/j.1399-0004.1999.550602.1.x

By:

Nasir, Jamal

Publication type:

Article

HotSpots: Neurogenesis challenges age old dogma.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 395, doi. 10.1034/j.1399-0004.1999.550602.2.x

By:

Nasir, Jamal

Publication type:

Article

HotSpots: Catch 22.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 396, doi. 10.1034/j.1399-0004.1999.550602.x

By:

Nasir, Jamal

Publication type:

Article

40 years of the annual ‘Bar Harbor Course’ (1960–1999): a pictorial history.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 398, doi. 10.1034/j.1399-0004.1999.550603.x

By:

McKusick, Victor A;
Naggert, Juergen;
Nishina, Patsy;
Valle, David

Publication type:

Article

Genetic landmarks through philately – hereditary breast cancer1.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 416, doi. 10.1034/j.1399-0004.1999.550604.x

By:

Chudley, Albert E

Publication type:

Article

Chromosome 11q13 and atopic asthma.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 431, doi. 10.1034/j.1399-0004.1999.550606.x

By:

Adra, C N;
Mao, X-Q;
Kawada, H;
Gao, P-S;
Korzycka, B;
Donate, J L;
Shaldon, S R;
Coull, P;
Dubowitz, M;
Enomoto, T;
Ozawa, A;
Syed, S A;
Horiuchi, T;
Khaeraja, R;
Khan, R;
Lin, S R;
Flinter, F;
Beales, P;
Hagihara, A;
Inoko, H

Publication type:

Article

Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 419, doi. 10.1034/j.1399-0004.1999.550605.x

By:

Cappelli, M;
Surh, L;
Humphreys, L;
Verma, S;
Logan, D;
Hunter, A;
Allanson, J

Publication type:

Article

Association between AGT codon 235 polymorphism and variation in serum concentrations of creatinine and urea in Canadian Oji-Cree.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 438, doi. 10.1034/j.1399-0004.1999.550607.x

By:

Hegele, Ra;
Harris, Sb;
Hanley, Ajg;
Zinman, B

Publication type:

Article

Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 444, doi. 10.1034/j.1399-0004.1999.550608.x

By:

Al-Jishi, E;
Meyer, Bf;
Rashed, Ms;
Al-Essa, M;
Al-Hamed, Mh;
Sakati, N;
Sanjad, S;
Ozand, Pt;
Kambouris, M

Publication type:

Article

A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease: the Framingham Offspring Study.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 450, doi. 10.1034/j.1399-0004.1999.550609.x

By:

Gagné, Se;
Larson, Mg;
Pimstone, Sn;
Schaefer, Ej;
Kastelein, Jjp;
Wilson, Pwf;
Ordovas, Jm;
Hayden, Mr

Publication type:

Article

Schizophrenia susceptibility gene locus at Xp22.3.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 455, doi. 10.1034/j.1399-0004.1999.550610.x

By:

Milunsky, Jeff;
Huang, Xin-Li;
Wyandt, Herman E;
Milunsky, Aubrey

Publication type:

Article

Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate gene.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 466, doi. 10.1034/j.1399-0004.1999.550612.x

By:

Ikegawa, Shiro;
Masuno, Mitsuo;
Kumano, Yoshiharu;
Okawa, Akihiko;
Isomura, Minoru;
Koyama, Kumiko;
Okui, Keiko;
Makita, Yoshio;
Sasaki, Michiko;
Kohdera, Urara;
Okuda, Masumi;
Koyama, Hirofumi;
Ohashi, Hirofumi;
Tajiri, Hitoshi;
Imaizumi, Kiyoshi;
Nakamura, Yusuke

Publication type:

Article

Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 461, doi. 10.1034/j.1399-0004.1999.550611.x

By:

Gehrig, Andrea;
White, Karen;
Lorenz, Birgit;
Andrassi, Monika;
Clemens, Stefan;
Weber, Bernhard Hf

Publication type:

Article

Further evidence from two families that craniofrontonasal dysplasia maps to Xp22.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 473, doi. 10.1034/j.1399-0004.1999.550613.x

By:

Pulleyn, Lj;
Winter, Rm;
Reardon, W;
McKeown, C;
Jones, B;
Hayward, R;
Evans, R;
Malcolm, S

Publication type:

Article

Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 478, doi. 10.1034/j.1399-0004.1999.550614.x

By:

Baud, Olivier;
Cormier-Daire, Valérie;
Lyonnet, Stanislas;
Desjardins, Laurence;
Turleau, Catherine;
Doz, François

Publication type:

Article

Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 483, doi. 10.1034/j.1399-0004.1999.550615.x

By:

Gyftodimou, J;
Karadima, G;
Pandelia, E;
Vassilopoulos, D;
Petersen, Mb

Publication type:

Article

A microdeletion syndrome due to a 3-Mb deletion on 19q13.2 – Diamond–Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation.

Published in:

Clinical Genetics, 1999, v. 55, n. 6, p. 487, doi. 10.1034/j.1399-0004.1999.550616.x

By:

Cario, H;
Bode, H;
Gustavsson, P;
Dahl, N;
Kohne, E

Publication type:

Article

Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation.

Published in:: 1999
Publication type:: Letter

Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screening.

Published in:

1999

By:

Frossard, Philippe M;
Lestringant, Gilles;
Girodon, Emmanuelle;
Goossens, Michel;
Dawson, Kenneth P

Publication type:

Letter