Works matching IS 00099163 AND DT 1992 AND VI 42 AND IP 5

Results: 12

Detection of the Pro.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 273, doi. 10.1111/j.1399-0004.1992.tb03255.x

By:

Defesche, J. C.;
Ree, M. A.;
Kastelein, J. J. P.;
Diermen, D. E.;
Janssens, N. W. E.;
Doormaal, J. J.;
Hayden, M. R.

Publication type:

Article

Deletion of 15q12 in Angelman syndrome: report of 3 new cases.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 229, doi. 10.1111/j.1399-0004.1992.tb03246.x

By:

Tonk, Vijay;
Wyandt, Herman E.;
Michand, Lucille;
Milunsky, Aubrey

Publication type:

Article

β-Thalassaemia mutations and their linkage to β-haplotypes in Tamil Nadu in Southern India.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 251, doi. 10.1111/j.1399-0004.1992.tb03250.x

By:

Venkatesan, Radha;
Sarkar, Rita;
Old, John M.

Publication type:

Article

The Dyggve-Melchior-Clausen syndrome in Indian siblings.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 240, doi. 10.1111/j.1399-0004.1992.tb03248.x

By:

Winship, W. S.;
Rubin, D. L.

Publication type:

Article

Analysis of three glucose transporter genes in a Caucasian population: no associations with non-insulin-dependent diabetes and obesity.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 260, doi. 10.1111/j.1399-0004.1992.tb03252.x

By:

Oelbaum, R. S.

Publication type:

Article

A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjects.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 224, doi. 10.1111/j.1399-0004.1992.tb03245.x

By:

Leren, Trond P.;
Solberg, Kari;
Røby, Oddveig;
Rødningen, Olaug K.;
Tonstad, Serena;
Ose, Leiv;
Berg, Kåre

Publication type:

Article

De novo interstitial deletion 16(q12. 1q13) of paternal origin in a 10-year-old boy.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 246, doi. 10.1111/j.1399-0004.1992.tb03249.x

By:

Schuffenhauer, Simone;
Callen, David F.;
Seidel, Heide;
Shen, Yang;
Lederer, Gabriele;
Murken, Jan

Publication type:

Article

Fertility in myotonic dystrophy in Saguenay-Lac-St-Jean: a historical perspective.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 234, doi. 10.1111/j.1399-0004.1992.tb03247.x

By:

Dao, To-Nga;
Mathieu, Jean;
Bouchard, Jean-Pierrs;
Braekeleer, Marc De

Publication type:

Article

Deletion ΔF508 and clinical expression of cystic fibrosis-related liver disease.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 271, doi. 10.1111/j.1399-0004.1992.tb03254.x

By:

Arce, M.;
O'Brien, S.;
Hegarty, J.;
O'Mahoney, S. M.;
Cashman, S. M.;
Martinez, A.;
Delgado, M.;
FitzGerald, M. X.

Publication type:

Article

StyI polymorphism in an enhancer region of the second intron of the apolipoprotein B gene in hyper- and hypocholesterolemic subjects.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 217, doi. 10.1111/j.1399-0004.1992.tb03244.x

By:

Røshy, Oddveig;
Poledne, Rudolf;
Hjermann, Ingvar;
Tonstad, Serena;
Berg, Kåre;
Leren, Trond P.

Publication type:

Article

A case of human chimerism detected by unbalanced chromosomal translocation.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 257, doi. 10.1111/j.1399-0004.1992.tb03251.x

By:

Nyberg, R. H.;
Haapala, A. K.;
Simola, K. O. J.

Publication type:

Article

Deciphering the fluorescent variability of human genomic heterochromatin by DA/DAPI technique.

Published in:

Clinical Genetics, 1992, v. 42, n. 5, p. 267, doi. 10.1111/j.1399-0004.1992.tb03253.x

By:

Verma, Ram S.;
Conte, Robert A.;
Luke, Sunay;
Sindwani, Veena;
Macera, Michael J.

Publication type:

Article