Works matching IS 00099163 AND DT 1975 AND VI 7 AND IP 2

Results: 14

Familial D/D translocation t(13q;14q) Eight members in four generations.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 91, doi. 10.1111/j.1399-0004.1975.tb00303.x

By:

Centerwall, Willard R.;
Merrell, Preston R.

Publication type:

Article

Alpha fetoprotein levels in maternal serum and in amniotic fluid from early normal pregnancies.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 170, doi. 10.1111/j.1399-0004.1975.tb00314.x

By:

Nørgaard-Pedersen, B.;
Lindsten, J.;
Philip, J.

Publication type:

Article

Amniotic fluid alphafetoprotein measurements in the early prenatal diagnosis of central nervous system disorders.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 163, doi. 10.1111/j.1399-0004.1975.tb00313.x

By:

Brock, D. J. H.;
Scrimgeour, I. B.;
Nelson, M. M.

Publication type:

Article

A new case of the trisomy 9p syndrome: Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p)) and a peculiar congenital heart defect.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 134, doi. 10.1111/j.1399-0004.1975.tb00309.x

By:

Orye, E.;
Verhaaren, H.;
Egmond, H. Van;
Devloo-Blancquaert, A.

Publication type:

Article

A new form of hereditary short limbed dwarf ism with microcephalus.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 111, doi. 10.1111/j.1399-0004.1975.tb00306.x

By:

Juberg, Richard C.;
Ness, Madge B. Van

Publication type:

Article

Genetics of acheiropodia ('the handless and footless families of Brazil').

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 98, doi. 10.1111/j.1399-0004.1975.tb00304.x

By:

Freire-Maia, Ademar

Publication type:

Article

Familial primary vesicoureteral reflux.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 144, doi. 10.1111/j.1399-0004.1975.tb00310.x

By:

Fried, K.;
Yuval, E.;
Eidelman, A.;
Beer, S.

Publication type:

Article

An XX male: Cytogenetic and endocrine studies.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 155, doi. 10.1111/j.1399-0004.1975.tb00312.x

By:

Rios, Maria E.;
Kaufman, Robert L.;
Sekhon, Gurbax S.;
Bucy, James G.;
Bauman, Joan E.;
Jacobs, Lawrence S.

Publication type:

Article

Isochromosome for the short arm of X: A human mosaic 45,X/46,XXpi.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 148, doi. 10.1111/j.1399-0004.1975.tb00311.x

By:

Fitzgerald, P. H.;
Donald, R. A.

Publication type:

Article

Incontinentia pigmenti.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 103, doi. 10.1111/j.1399-0004.1975.tb00305.x

By:

Iancu, T.;
Komlos, L.;
Shabtay, F.;
Elian, E.;
Halbrecht, I.;
Böök, J. A.

Publication type:

Article

Elevated levels of alfa fetoprotein in maternal serum and amniotic fluid in two cases of spina bifida.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 176, doi. 10.1111/j.1399-0004.1975.tb00315.x

By:

Malmqvist, E.;
Lindsten, J.;
Nørgaard-Pedersen, B.;
Hellström, B.;
Sundberg, B.

Publication type:

Article

A familial F/G translocation [t(20p-; 22q+)] observed in three generations.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 120, doi. 10.1111/j.1399-0004.1975.tb00307.x

By:

Cohen, Maimon M.;
Davidson, Ronald G.;
Brown, Judith A.

Publication type:

Article

A possible major contribution to mental retardation in the general population by the gene for microcephaly.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 85, doi. 10.1111/j.1399-0004.1975.tb00302.x

By:

Qazi, Qutub H.;
Reed, T. Edward

Publication type:

Article

Cystic fibrosis heterozygote detection: A study on a normal population.

Published in:

Clinical Genetics, 1975, v. 7, n. 2, p. 128, doi. 10.1111/j.1399-0004.1975.tb00308.x

By:

Danes, B. Shannon

Publication type:

Article