Works matching IS 00099163 AND DT 1985 AND VI 27 AND IP 2

Results: 19

Cystic fibrosis; hint of linkage with F13B.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 206, doi. 10.1111/j.1399-0004.1985.tb00213.x

By:

Eiberg, H.;
Schmiegelow, K.;
Koch, C.;
Mohr, J.;
Schwartz, M.;
Niebuhr, E.

Publication type:

Article

Diploid-tetraploid mosaicism in a malformed boy.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 183, doi. 10.1111/j.1399-0004.1985.tb00208.x

By:

Quiroz, E.;
Orozco, A.;
Salamanca, F.

Publication type:

Article

Familial nevus flammeus of the forehead and Unna's nevus.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 165, doi. 10.1111/j.1399-0004.1985.tb00205.x

By:

Merlob, Paul;
Reisner, Salomon H.

Publication type:

Article

Effect of balanced X/autosome translocations on sexual and physical development.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 147, doi. 10.1111/j.1399-0004.1985.tb00202.x

By:

Kleczkowska, A.;
Fryns, J. P.;
Vinken, L.;
Berghe, H. van den

Publication type:

Article

Decreased scattering coefficient of blue sclerae.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 187, doi. 10.1111/j.1399-0004.1985.tb00209.x

By:

Lanting, Peter J. H.;
Borsboom, Peter C. F.;
Meerman, Gerard J. te;
Kate, Leo P. ten

Publication type:

Article

Dermatoglyphic findings in patients with fragile X-chromosome.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 118, doi. 10.1111/j.1399-0004.1985.tb00197.x

By:

Hirth, L.;
Singh, S.;
Schilling, S.;
Müller, E.;
Goedde, H. W.

Publication type:

Article

A new lethal chondrodysplasia with spondylocostal dysostosis, multiple internal anomalies and Dandy-Walker cyst.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 160, doi. 10.1111/j.1399-0004.1985.tb00204.x

By:

Moerman, Ph.;
Vandenberghe, K.;
Fryns, J. P.;
Haspeslagh, M.;
Lauweryns, J. M.

Publication type:

Article

Frequency of the fragile X syndrome in infantile autism.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 113, doi. 10.1111/j.1399-0004.1985.tb00196.x

By:

Blomquist, Hans K:Son;
Bohman, Michael;
Edvinsson, Sven Olof;
Gillberg, Christopher;
Gustavson, Karl-Henrik;
Holmgren, Gösta;
Wahlström, Jan

Publication type:

Article

A distinct variant of intermediate maple syrup urine disease.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 153, doi. 10.1111/j.1399-0004.1985.tb00203.x

By:

Gonzalez-Rios, Maria del Carmen;
Chuang, David T.;
Cox, Rody P.;
Schmidt, Kathleen;
Knopf, Karen;
Packman, Seymour

Publication type:

Article

A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 175, doi. 10.1111/j.1399-0004.1985.tb00207.x

By:

Schwartz, S.;
Beisel, J. H.;
Panny, S. R.;
Cohen, M. M.

Publication type:

Article

Studies on human low serum IgD phenotype and Gm markers.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 134, doi. 10.1111/j.1399-0004.1985.tb00200.x

By:

Litwin, S. D.;
Tse-Eng, D.;
Jr, V. P. Butler;
Pernis, B.

Publication type:

Article

Supraumbilical midabdominal raphe and facial cavernous hemangiomas.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 196, doi. 10.1111/j.1399-0004.1985.tb00211.x

By:

Igarashi, M.;
Uchida, H.;
Kajii, T.

Publication type:

Article

Disease risk estimates from marker association data: Application to individuals at risk for hemochromatosis.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 127, doi. 10.1111/j.1399-0004.1985.tb00199.x

By:

Lin, Henry J.;
Conte, William J.;
Rotter, Jerome I.

Publication type:

Article

Tetraploidy in two sisters with the polycystic ovary syndrome.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 167, doi. 10.1111/j.1399-0004.1985.tb00206.x

By:

Rojanasakul, Aram;
Gustavson, Karl-Henrik;
Lithell, Hans;
Nillius, Sven Johan

Publication type:

Article

Semiautomated chromosome analysis: A clinical test.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 140, doi. 10.1111/j.1399-0004.1985.tb00201.x

By:

Philip, J.;
Lundsteen, C.

Publication type:

Article

The dysequilibrium syndrome: a study of the etiology and pathogenesis.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 191, doi. 10.1111/j.1399-0004.1985.tb00210.x

By:

Rasmussen, Finn;
Gustavson, Karl-Henrik;
Sara, Vicki R.;
Floderus, Ylva

Publication type:

Article

Oral and dental development in X chromosome aneuploidy.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 122, doi. 10.1111/j.1399-0004.1985.tb00198.x

By:

Farge, P.;
Dallaire, L.;
Albert, G.;
Melanĉon, S. B.;
Potter, M.;
Leboeuf, G.

Publication type:

Article

The Human Gene Map 1 December 1984.

Published in:: Clinical Genetics, 1985, v. 27, n. 2, p. 207, doi. 10.1111/j.1399-0004.1985.tb00214.x
Publication type:: Article

Ethical aspects of medical genetics.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 199, doi. 10.1111/j.1399-0004.1985.tb00212.x

By:

Fletcher, John C.;
Berg, Kåre;
Tranøy, Knut Erik

Publication type:

Article