Works matching IS 00099163 AND DT 1984 AND VI 25 AND IP 5

Results: 12

Differential diagnosis of the Williams and the Noonan syndromes.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 429, doi. 10.1111/j.1399-0004.1984.tb02012.x

By:

Preus, M.

Publication type:

Article

Ocular, cerebral and cutaneous malformations: confirmation of an association.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 464, doi. 10.1111/j.1399-0004.1984.tb02018.x

By:

Ferguson, James W.;
Hutchison, H. Terry;
Rouse, Bobbye M.

Publication type:

Article

The development of four unselected 47,XYY boys.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 435, doi. 10.1111/j.1399-0004.1984.tb02013.x

By:

Bender, Bruce G.;
Puck, Mary H.;
Salbenblatt, James A.;
Robinson, Arthur

Publication type:

Article

Myotonic dystrophy and autosomal balanced translocation t(2; 20) (p21; q11).

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 446, doi. 10.1111/j.1399-0004.1984.tb02014.x

By:

Fryns, J. P.;
Kleczkowska, A.;
Bulcke, I.;
Berghe, H.

Publication type:

Article

Orbital cyst in addition to congenital cerebral and focal dermal malformations: a new entity.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 470, doi. 10.1111/j.1399-0004.1984.tb02019.x

By:

Delleman, J. W.;
Oorthuys, J. W. E.;
Bleeker-Wagemakers, E. M.;
Haar, B. G. A. ter;
Ferguson, J. W.

Publication type:

Article

Chromosome fragility in Alzheimer's disease.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 416, doi. 10.1111/j.1399-0004.1984.tb02010.x

By:

Smith, Arabella;
Broe, G. A.;
Williamson, Michael

Publication type:

Article

Partial Trisomy 9q resulting from a familial translocation t(9;16)(q32;q24).

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 449, doi. 10.1111/j.1399-0004.1984.tb02015.x

By:

Soltan, H. C.;
Jung, J. H.;
Pyatt, Z.;
Singh, R. P.

Publication type:

Article

The Williams syndrome: objective definition and diagnosis.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 422, doi. 10.1111/j.1399-0004.1984.tb02011.x

By:

Preus, M.

Publication type:

Article

Craniofrontonasal dysplasia - a distinct entity with lethality in the male?

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 473, doi. 10.1111/j.1399-0004.1984.tb02020.x

By:

Young, I. D.;
Moore, J. R.

Publication type:

Article

Interstitial deletion of band q12 of chromosome 5.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 455, doi. 10.1111/j.1399-0004.1984.tb02016.x

By:

Dudin, Gertrud;
Alexander, Denis;
Talj, Fayrouz;
Deeb, Mary;
Musallam, Salim;
Kaloustian, Vazken M. Der

Publication type:

Article

Clinical consequences of heterozygosity for autosomal-recessive diseases*,**.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 381, doi. 10.1111/j.1399-0004.1984.tb02009.x

By:

Vogel, F.

Publication type:

Article

Abnormal B.A.E.P. in a family with Moebius syndrome: evidence for supranuclear lesion.

Published in:

Clinical Genetics, 1984, v. 25, n. 5, p. 459, doi. 10.1111/j.1399-0004.1984.tb02017.x

By:

Stabile, M.;
Cavaliere, M. L.;
Scarano, G.;
Fels, A.;
Valianl, R.;
Ventruto, V.

Publication type:

Article