Works matching IS 00099163 AND DT 2000 AND VI 57 AND IP 1

Results: 19

‘New Age’ gene medicines for the 21st century.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 11, doi. 10.1034/j.1399-0004.2000.570102.x

By:

Suzanne Lewis, ME

Publication type:

Article

The success of gene therapy in correcting the failings of advancing age.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 13, doi. 10.1034/j.1399-0004.2000.5701022.x

By:

Suzanne Lewis, ME

Publication type:

Article

Caspases and neurodegeneration: on the cutting edge of new therapeutic approaches.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 1, doi. 10.1034/j.1399-0004.2000.570101.x

By:

Wellington, Cheryl L;
Hayden, Michael R

Publication type:

Article

Genetic modification of the human mitotic clock by telomerase: a matter of life and death.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 11, doi. 10.1034/j.1399-0004.2000.5701021.x

By:

Suzanne Lewis, ME

Publication type:

Article

The molecular regulation of myogenesis.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 16, doi. 10.1034/j.1399-0004.2000.570103.x

By:

Sabourin, Luc A;
Rudnicki, Michael A

Publication type:

Article

Genetic landmarks through philately – Crick, Watson and Wilkins: the scientists behind DNA structure.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 26, doi. 10.1034/j.1399-0004.2000.570104.x

By:

Chudley, Albert E

Publication type:

Article

Support for linkage of familial combined hyperlipidemia to chromosome 1q21–q23 in Chinese and German families.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 29, doi. 10.1034/j.1399-0004.2000.570105.x

By:

Pei, Weidong;
Baron, Heike;
Müller-Myhsok, Bertram;
Knoblauch, Hans;
Ali Al-Yahyaee, Said;
Hui, Rutai;
Wu, Xigui;
Liu, Lisheng;
Busjahn, Andreas;
Luft, Friedrich C;
Schuster, Herbert

Publication type:

Article

Impact of age and body size on inter-individual variation in measures of lipid metabolism: influence of gender and apolipoprotein E genotype.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 35, doi. 10.1034/j.1399-0004.2000.570106.x

By:

Lussier-Cacan, S;
Bolduc, A;
Xhignesse, M;
Niyonsenga, T;
Connelly, PW;
Sing, CF

Publication type:

Article

Assessment of education and counselling offered by a familial colorectal cancer clinic.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 48, doi. 10.1034/j.1399-0004.2000.570107.x

By:

Collins, Veronica;
Halliday, Jane;
Warren, Rosemary;
Williamson, Robert

Publication type:

Article

Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 56, doi. 10.1034/j.1399-0004.2000.570108.x

By:

Żebrak, Jerzy;
Skuza, Barbara;
Pogorzelski, Andrzej;
Ligarska, Renata;
Kopytko, Ewa;
Pawlik, Jacek;
Rutkiewicz, Ewa;
Witt, Michal

Publication type:

Article

An SRY-negative XX male with Huriez syndrome.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 61, doi. 10.1034/j.1399-0004.2000.570109.x

By:

Vernole, Patrizia;
Terrinoni, Alessandro;
Didona, Biagio;
De Laurenzi, Vincenzo;
Rossi, Pellegrino;
Melino, Gerry;
Grimaldi, Paola

Publication type:

Article

Identification of three novel mutations in the insulin receptor gene in type A insulin resistant patients.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 67, doi. 10.1034/j.1399-0004.2000.570110.x

By:

Riqué, Susanna;
Nogués, Carme;
Ibàñez, Lourdes;
Victoria Marcos, María;
Ferragut, Juan;
Carrascosa, Antonio;
Potau, Neus

Publication type:

Article

Correlations between individual clinical manifestations and CTG repeat amplification in myotonic dystrophy.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 74, doi. 10.1034/j.1399-0004.2000.570112.x

By:

Marchini, Corrado;
Lonigro, Renata;
Verriello, Lorenzo;
Pellizzari, Lucia;
Bergonzi, Paolo;
Damante, Giuseppe

Publication type:

Article

An unaffected individual from a breast/ovarian cancer family with germline mutations in both BRCA1 and BRCA2.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 70, doi. 10.1034/j.1399-0004.2000.570111.x

By:

Moslehi, Roxana;
Russo, Donna;
Phelan, Catherine;
Jack, Elaine;
Antman, Karen;
Narod, Steven

Publication type:

Article

The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 83, doi. 10.1034/j.1399-0004.2000.570113.x

By:

Devriendt, Koenraad;
Holvoet, Maureen;
De Mûelenaere, Alain;
Fryns, Jean-Pierre

Publication type:

Article

A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 86, doi. 10.1034/j.1399-0004.2000.570114.x

By:

Fridman, Cintia;
Santos, Mara;
Ferrari, Íris;
Koiffmann, Célia P

Publication type:

Article

‘Novel’ immunodeficiency syndrome may be a previously described entity.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 90, doi. 10.1034/j.1399-0004.2000.570116.x

By:

Carpenter, Nancy J;
Berkel, Izzet;
Say, Burhan

Publication type:

Article

The International Federation of Human Genetics Societies.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 88, doi. 10.1034/j.1399-0004.2000.570115.x

By:

Ayme, Segolene

Publication type:

Article

Reply to the letter by Carpenter et al. ‘Novel’ immunodeficiency syndrome may be a previously described entity.

Published in:

Clinical Genetics, 2000, v. 57, n. 1, p. 91, doi. 10.1034/j.1399-0004.2000.570117.x

By:

Roifman, Chaim M

Publication type:

Article