Works matching IS 00099163 AND DT 1994 AND VI 46 AND IP 3

Results: 12

Determination of haemophilia A carrier status from hair samples using polymerase chain reaction technique.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 263, doi. 10.1111/j.1399-0004.1994.tb04239.x

By:

Hussain, S.;
Shamim, A.;
Vencer, L.;
Butt, A. I.;
Al-Harithy, R.;
Nasim, A.

Publication type:

Article

A 12-year preventive program for β-thalassemia in Northern Sardinia.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 238, doi. 10.1111/j.1399-0004.1994.tb04233.x

By:

Longinotti, M.;
Pistidda, P.;
Oggiano, L.;
Guiso, L.;
Frogheri, L.;
Dore, F.;
Pardini, S.;
Bonfigli, S.;
Rimini, E.;
Angioni, S.;
Mulas, P.;
Inzaina, A.

Publication type:

Article

Inv dup(15): contribution to the clinical definition of phenotype.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 233, doi. 10.1111/j.1399-0004.1994.tb04232.x

By:

Grammatico, P.;
Rosa, C.;
Roccella, M.;
Falcolini, M.;
Pelliccia, A.;
Roccella, F.;
Porto, G.

Publication type:

Article

Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 244, doi. 10.1111/j.1399-0004.1994.tb04234.x

By:

Lurie, Iosif W.;
Wulfsberg, Eric A.;
Prabhakar, Gayathri;
Rosenblum-Vos, Lynne S.;
Supovitz, Karen R.;
Cohen, Maimon M.

Publication type:

Article

Possible localization of a major gene for cleft lip and palate to 4q.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 255, doi. 10.1111/j.1399-0004.1994.tb04236.x

By:

Beiraghi, S.;
Foroud, T.;
Diouhy, S.;
Bixler, D.;
Conneally, P. M.;
Delozier-Blanchet, D.;
Hodes, M. E.

Publication type:

Article

DNA polymorphisms of human apolipoprotein A-IV gene: frequency and effects on lipid, lipoprotein and apolipoprotein levels in a French population.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 248, doi. 10.1111/j.1399-0004.1994.tb04235.x

By:

Zaiou, Mohamed;
Visvikis, Sophia;
Gueguen, René;
Parra, Henri-Joseph;
Fruchart, Jean Charles;
Siest, Gérard

Publication type:

Article

Unilateral renal aplasia in X-linked Kallmann's syndrome.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 260, doi. 10.1111/j.1399-0004.1994.tb04238.x

By:

Kirk, J. M. W.;
Grant, D. B.;
Besser, G. M.;
Shalet, S.;
Quinton, R.;
Smith, C. S.;
White, M.;
Edwards, O.;
Bouloux, P.-M. G.

Publication type:

Article

A case of de novo interstitial deletion of chromosome 9(p12p13).

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 271, doi. 10.1111/j.1399-0004.1994.tb04241.x

By:

Giltay, Jacques C.;
Gerssen-Schoorl, Klasien B. J.;
Wagen, Ab

Publication type:

Article

DNA polymorphisms at the locus for human cholesteryl ester transfer protein (CETP) are associated with macro- and microangiopathy in non-insulin-dependent diabetes mellitus.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 217, doi. 10.1111/j.1399-0004.1994.tb04230.x

By:

Ukkola, Olavi;
Savolainen, Markku J.;
Salmela, Pasi I.;
Dickhoff, Kai;
Kesäniemi, Y. Antero

Publication type:

Article

Exclusion of linkage to 14q23-24 in a family with Holt-Oram syndrome.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 257, doi. 10.1111/j.1399-0004.1994.tb04237.x

By:

Ruiz, Juan Carlos;
Legius, Eric;
Cuppens, Harry;
Moens, Pierre;
Marynen, Peter;
Cassiman, Jean-Jacques

Publication type:

Article

Linkage between severe atopy and chromosome 11q13 in Japanese families.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 228, doi. 10.1111/j.1399-0004.1994.tb04231.x

By:

Shirakawa, T.;
Hashimoto, T.;
Furuyama, J.;
Takeshita, T.;
Morimoto, K.

Publication type:

Article

Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotype.

Published in:

Clinical Genetics, 1994, v. 46, n. 3, p. 268, doi. 10.1111/j.1399-0004.1994.tb04240.x

By:

Digilio, M. C.;
Mingarelli, R.;
Marino, B.;
Giannotti, A.;
Melchionda, S.;
Dallapiccola, B.

Publication type:

Article