Works matching IS 00099163 AND DT 1985 AND VI 28 AND IP 2

Results: 20

The Eighth Annual New York March of Dimes Symposium on Genetics for the Practicing Physician.

Published in:: Clinical Genetics, 1985, v. 28, n. 2, p. 183, doi. 10.1111/j.1399-0004.1985.tb00384.x
Publication type:: Article

Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 136, doi. 10.1111/j.1399-0004.1985.tb00373.x

By:

Söderholm, Anna-Lisa;
Kaitila, Ilkka

Publication type:

Article

The cerebro-costo-mandibular syndrome: third report of familial occurrence.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 118, doi. 10.1111/j.1399-0004.1985.tb00370.x

By:

Hennekam, R. C. M.;
Beemer, F. A.;
Huijbers, W. A. R.;
Hustinx, P. A.;
Sprang, F. J. van

Publication type:

Article

Frequency of fragile X chromosome in normal females.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 97, doi. 10.1111/j.1399-0004.1985.tb00366.x

By:

Abuelo, Dunne;
Castree, Katherine;
Pueschel, Siegfried;
Padre-Mendoza, Teresita;
Zolnierz, Kathy

Publication type:

Article

Heterogeneity of Kallmann's syndrome.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 106, doi. 10.1111/j.1399-0004.1985.tb00368.x

By:

Hermanussen, M.;
Sippell, W. G.

Publication type:

Article

Cornelia de Lange syndrome in a mother and daughter.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 157, doi. 10.1111/j.1399-0004.1985.tb00376.x

By:

Leavitt, Anne;
Dinno, Nuhad;
Davis, Catherine

Publication type:

Article

Imaging techniques in muscular dystrophies.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 179, doi. 10.1111/j.1399-0004.1985.tb00382.x

By:

Rott, Hans-Dieter;
Rödl, Werner

Publication type:

Article

EEC syndrome without ectrodactyly? Report of 8 cases.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 130, doi. 10.1111/j.1399-0004.1985.tb00372.x

By:

Küster, W.;
Majewski, F.;
Meinecke, P.

Publication type:

Article

Partial trisomy 12q: clinical and cytogenetic observations.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 112, doi. 10.1111/j.1399-0004.1985.tb00369.x

By:

Tengström, C.;
Wilska, M.;
Kähkönen, M.;
Autio, S.;
Leisti, J.

Publication type:

Article

Heritable fragility at 11q13 and 12q13.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 145, doi. 10.1111/j.1399-0004.1985.tb00374.x

By:

Smeets, D. F. C. M.;
Scheres, J. M. J. C.;
Hustinx, T. W. J.

Publication type:

Article

46, X, i(Xq) karyotype in a patient with hypoplastic left heart.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 178, doi. 10.1111/j.1399-0004.1985.tb00381.x

By:

Shah, Ashok;
Fay, John E.;
Ford, Sally;
Holden, Jeanette J. A.

Publication type:

Article

13th Annual Meeting of the European Working Group for Cystic Fibrosis.

Published in:: Clinical Genetics, 1985, v. 28, n. 2, p. 183, doi. 10.1111/j.1399-0004.1985.tb00385.x
Publication type:: Article

Age of onset in siblings of persons with juvenile Huntinqton disease.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 100, doi. 10.1111/j.1399-0004.1985.tb00367.x

By:

Hayden, M. R.;
Soles, J. A.;
Ward, D R. H.

Publication type:

Article

Prenatal testing and twinning.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 180, doi. 10.1111/j.1399-0004.1985.tb00383.x

By:

Flannery, David B.;
Holzman, Gerald B.

Publication type:

Article

Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritance.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 151, doi. 10.1111/j.1399-0004.1985.tb00375.x

By:

Somer, Hannu;
Voutilainen, Arja;
Knuutila, Sakari;
Kaitila, Ilkka;
Rapola, Juhani;
Leinonen, Hannu

Publication type:

Article

Partial trisomy 5q and partial monosomy 5q within the same family.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 122, doi. 10.1111/j.1399-0004.1985.tb00371.x

By:

Lazjuk, G. I.;
Lurie, I. W.;
Kirillova, I. A.;
Zaletajev, D. V.;
Gurevich, D. B.;
Shved, I. A.;
Ostrovskaya, T. I.

Publication type:

Article

An unusual variant chromosome 9 with an extra C-negative, G-dark segment in the short arm.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 162, doi. 10.1111/j.1399-0004.1985.tb00377.x

By:

Spedicato, F. S.;
Comite, A. Di;
Tohidast-Akrad, M.

Publication type:

Article

A new banding pattern of human chromosomes by in situ nick translation using ECO RI and biotin-dUTP.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 173, doi. 10.1111/j.1399-0004.1985.tb00379.x

By:

Bullerdiek, Jörn;
Dittmer, Jürgen;
Faehre, Angelika;
Bartnitzke, Sabine;
Kasche, Volker;
Schloot, Werner

Publication type:

Article

A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 166, doi. 10.1111/j.1399-0004.1985.tb00378.x

By:

Romain, D. R.;
Columbano-Green, L. M.;
Parfitt, R. G.;
Chapman, C. J.;
Smythe, R. H.;
Gebbie, O. B.

Publication type:

Article

About diploid-tetraploid mosaicism.

Published in:

Clinical Genetics, 1985, v. 28, n. 2, p. 177, doi. 10.1111/j.1399-0004.1985.tb00380.x

By:

Chamla, Y.

Publication type:

Article