Works matching IS 00099163 AND DT 1986 AND VI 29 AND IP 4

Results: 15

Gonadoblastoma and Y-chromosome fluorescence.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 311, doi. 10.1111/j.1399-0004.1986.tb01259.x

By:

Lukusa, T.;
Fryns, J. P.;
Berghe, H. van den

Publication type:

Article

Deleted ring chromosome 22 in a mentally retarded boy.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 337, doi. 10.1111/j.1399-0004.1986.tb01264.x

By:

Gustavson, K.-H.;
Arancibia, W.;
Eriksson, U.;
Svennerholm, L.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1986, v. 29, n. 4, p. 348, doi. 10.1111/j.1399-0004.1986.tb01268.x
Publication type:: Article

The McCune-Albright syndrome: a lethal gene surviving by mosaicism.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 321, doi. 10.1111/j.1399-0004.1986.tb01261.x

By:

Happle, R.

Publication type:

Article

Trichodermodysplasia with dental alterations: an apparently new genetic ectodermal dysplasia of the trichoodonto-onychial subgroup.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 332, doi. 10.1111/j.1399-0004.1986.tb01263.x

By:

Pinheiro, Marta;
Freire-Maia, Dértia V.;
Miranda, E.;
Silva-Filho, O. G.;
Maia, N. Freire-

Publication type:

Article

Heterogeneity of Morquio disease.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 325, doi. 10.1111/j.1399-0004.1986.tb01262.x

By:

Beck, M.;
Glössl, J.;
Grubisic, A.;
Spranger, J.

Publication type:

Article

Measurement of body fat in Turner syndrome.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 291, doi. 10.1111/j.1399-0004.1986.tb01257.x

By:

Delgado, J. A.;
Trahms, C. M.;
Sybert, V. P.

Publication type:

Article

Absent tibiae, triphalangeal thumbs, Polydactyly and non-penetrance.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 347, doi. 10.1111/j.1399-0004.1986.tb01267.x

By:

Sonia Canún, S.

Publication type:

Article

Psychosocial adjustment of adult women with Turner syndrome.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 284, doi. 10.1111/j.1399-0004.1986.tb01256.x

By:

McCauley, Elizabeth;
Sybert, Virginia P.;
Ehrhardt, Anke A.

Publication type:

Article

Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20mosaicism.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 342, doi. 10.1111/j.1399-0004.1986.tb01265.x

By:

Holzgreve, Wolfgang;
Golabi, Mahin;
Bradley, Joel

Publication type:

Article

The Borjeson-Fbrssman-Lehmann syndrome.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 317, doi. 10.1111/j.1399-0004.1986.tb01260.x

By:

Dereymaeker, A. M.;
Fryns, J. P.;
Hoefnagels, M.;
Heremans, G.;
Marien, J.;
Berghe, H. van den

Publication type:

Article

Cardiovascular manifestations in Fabry's disease.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 276, doi. 10.1111/j.1399-0004.1986.tb01255.x

By:

Sakuraba, Hitoshi;
Yanagawa, Yukishige;
Igarashi, Takashi;
Suzuki, Yoshiyuki;
Suzuki, Tadashi;
Watanabe, Koji;
Ieki, Keiko;
Shimoda, Kosuke;
Yamanaka, Tatsuhiro

Publication type:

Article

The spectrum of clinical features in CHARGE syndrome.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 298, doi. 10.1111/j.1399-0004.1986.tb01258.x

By:

Davenport, Sandra L. H.;
Hefner, Margaret A.;
Mitchell, Joyce A.

Publication type:

Article

Congenital heart disease in supernumerary der(22), t(11;22) syndrome.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 269, doi. 10.1111/j.1399-0004.1986.tb01254.x

By:

Lin, Angela E.;
Bernar, Juan;
Chin, Alvin J.;
Sparkes, Robert S.;
Emanuel, Beverly S.;
Zackai, Elaine H.

Publication type:

Article

Incidence of trisomy 18 in Sweden in 1981-1982: Clustering in a small region.

Published in:

Clinical Genetics, 1986, v. 29, n. 4, p. 345, doi. 10.1111/j.1399-0004.1986.tb01266.x

By:

Annerén, G.

Publication type:

Article