Works matching IS 00015652 AND DT 1995 AND VI 45 AND IP 3

Results: 13

Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 121, doi. 10.1159/000154272

By:

Pericak-Vance, Margaret A.;
Barker, David F.;
Bergoffen, JoAnn;
Chance, Phillip;
Cochrane, Susan;
Dahl, Niklas;
Exler, Mareike-Christine;
Fain, Pamela R.;
Fairweather, Nicholas D.;
Fischbeck, Kenneth;
Gal, Andreas;
Haites, Neva;
Ionasescu, R.;
Ionasescu, Victor V.;
Kennerson, Marina L.;
Monaco, Anthony P.;
Mostaccuiolo, M.;
Nicholson, Garth A.;
Sillén, Anna;
Haines, Jonathan L.

Publication type:

Article

Description and Analysis of Allele Distribution for Four VNTR Markers in French and French Canadian Populations.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 135, doi. 10.1159/000154274

By:

Monson, Keith L.;
Moisan, Jean-Paul;
Pascal, Olivier;
McSween, Michèle;
Aubert, Dominique;
Giusti, Alan;
Budowle, Bruce;
Lavergne, Léo

Publication type:

Article

p53 Polymorphisms and Haplotypes in Different Ethnic Groups.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 144, doi. 10.1159/000154275

By:

Själander, A.;
Birgander, R.;
Kivelä, A.;
Beckman, G.

Publication type:

Article

Genetic Interactions and the Environment: A Study of ADA and ACP1 Systems in the Sardinian Population.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 129, doi. 10.1159/000154273

By:

Gloria-Bottini, F.;
Borgiani, P.;
Amante, A.;
Lucarelli, P.;
Bottini, E.

Publication type:

Article

Polymorphic Gene Markers in Mexican-Americans Residing in Southern California.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 150, doi. 10.1159/000154276

By:

Shohat, Tami;
Shaw, Sylvia J.;
Sparkes, Robert S.;
Vadheim, Constance M.;
Rotter, Jerome.I.;
Zeidler, Adina

Publication type:

Article

Complex Segregation Analysis in a Sample of Consecutive Newborns with Cleft Lip with or without Cleft Palate in Italy.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 157, doi. 10.1159/000154277

By:

Clementi, Maurizio;
Tenconi, Romano;
Collins, Andrew;
Calzolari, Elisa;
Milan, Mario

Publication type:

Article

Reply.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 179, doi. 10.1159/000154283

By:

Weeks, Daniel E.

Publication type:

Article

Announcement.

Published in:: Human Heredity, 1995, v. 45, n. 3, p. 164, doi. 10.1159/000154278
Publication type:: Article

Manic-Depression and the Norepinephrine Transporter Gene.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 165, doi. 10.1159/000154279

By:

Hadley, D.;
Hoff, M.;
Holik, J.;
Reimherr, F.;
Wender, P.;
Coon, H.;
Byerley, W.

Publication type:

Article

Study of 12 Mutations in Turkish Cystic Fibrosis Patients.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 175, doi. 10.1159/000154281

By:

Yılmaz, E.;
Erdem, H.;
Özgüç, M.;
Coskun, T.;
Özçelik, U.;
Göçmen, A.;
Özalp, İ.

Publication type:

Article

Linkage Analysis with Biological Markers.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 169, doi. 10.1159/000154280

By:

Ott, Jurg

Publication type:

Article

Applicability of the Rao Mapping Function.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 178, doi. 10.1159/000154282

By:

Morton, Newton E.

Publication type:

Article

Reply.

Published in:

Human Heredity, 1995, v. 45, n. 3, p. 180, doi. 10.1159/000154284

By:

Morton, Newton E.

Publication type:

Article