Works matching IS 00099163 AND DT 1980 AND VI 18 AND IP 1

Results: 18

Autosomal dominant and X-linked ichthyosis in the same family. Biochemical analysis of steroid sulfatase activity.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 48, doi. 10.1111/j.1399-0004.1980.tb01364.x

By:

Migl, B.;
Mevorah, B.;
Müller, C. R.;
Wolff, G.;
Frenk, E.

Publication type:

Article

Omphalocele in half-siblings.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 88, doi. 10.1111/j.1399-0004.1980.tb01370.x

By:

Kapur, Saroj;
Higgins, James V.;
Scott-Emuakpor, Ajovi B.;
Dolanski, Eugene A.

Publication type:

Article

Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 83, doi. 10.1111/j.1399-0004.1980.tb01369.x

By:

Schroer, Richard J.;
Culp, Donna M.;
Stevenson, Roger E.;
Potts, William E.;
Taylor, Harold A.;
Simensen, Richard J.

Publication type:

Article

Three levels of G-band differentiation.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 65, doi. 10.1111/j.1399-0004.1980.tb01367.x

By:

Sit, K. H.

Publication type:

Article

Clinical, hematological and genetic features of sickle-cell anemia and sickle cell-β thalassemia in a Brazilian population.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 58, doi. 10.1111/j.1399-0004.1980.tb01366.x

By:

Zago, M. A.;
Costa, F. F.;
Freitas, T. C.;
Bottura, C.

Publication type:

Article

The Wolf-Hirschhorn syndrome.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 6, doi. 10.1111/j.1399-0004.1980.tb01357.x

By:

Lazjuk, G. I.;
Lurie, I. W.;
Ostrowskaja, T. I.;
Kirillova, I. A.;
Nedzved, M. K.;
Cherstvoy, E. D.;
Silyaeva, N. F.

Publication type:

Article

Trisomy 18q-. Trisomy mapping of chromosome 18 revisited.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 20, doi. 10.1111/j.1399-0004.1980.tb01359.x

By:

Turleau, C.;
Chavin-Colin, F.;
Narbouton, R.;
Asensi, D.;
Grouchy, J. DE

Publication type:

Article

Prader-Willi syndrome and a bisatellited derivative of chromosome 15.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 42, doi. 10.1111/j.1399-0004.1980.tb01363.x

By:

Wisniewski, Lawrence P.;
Witt, Mary E.;
Ginsberg-Fellner, Fredda;
Wilner, Judith;
Desnick, Robert J.

Publication type:

Article

Immunoglobulin concentration and Gm allotypes in a family with thirty-three cases of myotonic dystrophy.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 13, doi. 10.1111/j.1399-0004.1980.tb01358.x

By:

Larsen, B.;
Johnson, G.;
Loghem, E. VAN;
Marshall, W. H.;
Newton, R. M.;
Pryse-Phillips, W.;
Skanes, V.

Publication type:

Article

Bloom's syndrome, missing Y, hypogonadism and cancer.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 93, doi. 10.1111/j.1399-0004.1980.tb01372.x

By:

Shabtai, Fiorella;
Halbrecht, Isaac

Publication type:

Article

Prenatal diagnosis of the prune belly syndrome.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 79, doi. 10.1111/j.1399-0004.1980.tb01368.x

By:

Bovicelli, Luciano;
Rizzo, Nicola;
Orsini, Luigi Fiuppo;
Michelacci, Laura

Publication type:

Article

Fetal gonadal histology in XXXXY, XYY and XXX syndromes.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 1, doi. 10.1111/j.1399-0004.1980.tb01356.x

By:

Autio-Harmainen, H.;
Rapola, J.;
Aula, P.

Publication type:

Article

Pericentric X chromosome ascertained during antenatal diagnosis.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 30, doi. 10.1111/j.1399-0004.1980.tb01361.x

By:

Evans, Mark I.;
Simpson, Joe Leigh;
Larsons, John W.;
Martin, Alice O.;
Sarto, Gloria E.;
Schulman, Joseph D.

Publication type:

Article

Binary developmental commitments in normal and abnormal human morphogenesis.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 34, doi. 10.1111/j.1399-0004.1980.tb01362.x

By:

Friedman, J. M.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1980, v. 18, n. 1, p. 96, doi. 10.1111/j.1399-0004.1980.tb01373.x
Publication type:: Article

Familial occurrence of trophoblastic disease - report of recurrent molar pregnancies in sisters in three families.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 27, doi. 10.1111/j.1399-0004.1980.tb01360.x

By:

Ambani, L. M.;
Vaidya, R. A.;
Rao, C. S.;
Daftary, S. D.;
Motashaw, N. D.

Publication type:

Article

Application of the lod score method to detection of linkage between HLA and juvenile insulin-dependent diabetes.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 51, doi. 10.1111/j.1399-0004.1980.tb01365.x

By:

Cleroet-Darpoux, F.;
Bonaiti-Pellie, C.;
Hors, J.;
Deschamps, I.;
Peingold, N.

Publication type:

Article

Waardenburg's Syndrome and Hirschsprung's Disease in the same Patient.

Published in:

Clinical Genetics, 1980, v. 18, n. 1, p. 91, doi. 10.1111/j.1399-0004.1980.tb01371.x

By:

Ph.D, K. Fried M.D.;
MD, S. Beer

Publication type:

Article