Works matching IS 00099163 AND DT 1990 AND VI 37 AND IP 1

Results: 15

Serum protein markers in Chinese schizophrenics - haptoglobin types and transferrin and group-specific component subtypes.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 54, doi. 10.1111/j.1399-0004.1990.tb03390.x

By:

Tsoi, N. Saha and W. F.

Publication type:

Article

A new syndrome of familial short stature, small hands, valvular heart disease and a characteristic facies.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 18, doi. 10.1111/j.1399-0004.1990.tb03385.x

By:

Collins, F. A.;
Partington, M. W.;
Mulcahy, D.;
Turner, G.

Publication type:

Article

Premature centromeric divisions and prominent telomeres in a patient with persistent Mullerian duct syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 69, doi. 10.1111/j.1399-0004.1990.tb03393.x

By:

Rangnekar, G. V.;
Loya, B. M.;
Goswami, L. K.;
Sengupta, L. K.

Publication type:

Article

Consanguinity and the genetic control of Down syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 24, doi. 10.1111/j.1399-0004.1990.tb03386.x

By:

Hamamy, Hanan A.;
Al-Hakkak, Zuhair S.;
Al-Taha, Salma

Publication type:

Article

Skin mastocytosis with short stature, conductive hearing loss and microtia: a new syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 64, doi. 10.1111/j.1399-0004.1990.tb03392.x

By:

Wolach, B.;
Raas-Rothschild, A.;
Metzker, A.;
Choc, L.;
Straussberg, R.;
Lew, S.;
Goodman, R. M.

Publication type:

Article

Maternal serum markers in screening for Down syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 35, doi. 10.1111/j.1399-0004.1990.tb03388.x

By:

Nørgaard-Pedersen, Bent;
Larsen, Severin Olesen;
Arends, Jørgen;
Svenstrup, Birgit;
Tabor, Ann

Publication type:

Article

Charcot-Marie-Tooth disease: call for patients.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 79, doi. 10.1111/j.1399-0004.1990.tb03396.x

By:

Broeckhoven, Christine

Publication type:

Article

Diagnostic molecular genetics of the fragile X.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 2, doi. 10.1111/j.1399-0004.1990.tb03383.x

By:

Sutherland, Grant R.;
Mulley, John C.

Publication type:

Article

Metachromatic leukodystrophy in Greece: observations on 4 cases.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 30, doi. 10.1111/j.1399-0004.1990.tb03387.x

By:

Michelakakis, Helen;
Dimitriou, Evagelia;
Bartsocas, Ch.;
Skardoutsou, Angeliki;
Giouroukos, S.

Publication type:

Article

RFLP analysis for diagnosis of haemophilia A in the German Democratic Republic.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 12, doi. 10.1111/j.1399-0004.1990.tb03384.x

By:

Herrmann, F. H.;
Wehnert, M.;
Wulff, K.

Publication type:

Article

Lack of specificity of DA/DAPI fluorescence.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 74, doi. 10.1111/j.1399-0004.1990.tb03394.x

By:

Lin, M. S.;
Huynh, K. H.;
Fujimoto, A.;
Wilson, M. G.

Publication type:

Article

Radial ray defects and associated anomalies; unique nature of the radial deficiencies and facial dysmorphism in the TAR syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 78, doi. 10.1111/j.1399-0004.1990.tb03395.x

By:

Lipson, Anthony

Publication type:

Article

Molecular Genetics of Diseases: Clinical Applications.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 1, doi. 10.1111/j.1399-0004.1990.tb03382.x

By:

Mohr, Jan

Publication type:

Article

Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 44, doi. 10.1111/j.1399-0004.1990.tb03389.x

By:

Nichols, William C.;
Benson, Merrill D.

Publication type:

Article

Clinical considerations in Buschke-Ollendorff syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 1, p. 59, doi. 10.1111/j.1399-0004.1990.tb03391.x

By:

Walpole, Ian R.;
Manners, Prudence J.

Publication type:

Article