Works matching IS 00099163 AND DT 1984 AND VI 26 AND IP 3

Results: 34

THIRD NORDIC CONFERENCE Pepsinogen and gastric cancer.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 240, doi. 10.1111/j.1399-0004.1984.tb04377.x

By:

Frants, Rune R.;
Pronk, Jan C.;
Pals, Gerard;
Defize, Jacques;
Westerveld, Benedict D.;
Meuwissen, Stefan G. M.;
Eriksen, Aldur W.

Publication type:

Article

Endocrine Genetics and Genetics of Growth.

Published in:: Clinical Genetics, 1984, v. 26, n. 3, p. 280, doi. 10.1111/j.1399-0004.1984.tb04396.x
Publication type:: Article

Diagnostic transcervical chorionic biopsles in first trimester pregnancies.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 262, doi. 10.1111/j.1399-0004.1984.tb04386.x

By:

Marsk, L.;
Søndergaard, F.;
Secher, J.;
Lindsten, J.;
Mikkelsen, M.

Publication type:

Article

Analysis of a familial 15p + polymorphism: exclusion of Y/15 translocation.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 204, doi. 10.1111/j.1399-0004.1984.tb04368.x

By:

Werner, W.;
Herrmann, F. H.

Publication type:

Article

Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 174, doi. 10.1111/j.1399-0004.1984.tb04364.x

By:

Hecht, Frederick;
Hecht, Barbara K.

Publication type:

Article

Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variations.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 178, doi. 10.1111/j.1399-0004.1984.tb04365.x

By:

Annerhn, G.;
Arvidson, B.;
Gustavson, K-H.;
Jorulf, H.;
Carlsson, G.

Publication type:

Article

Prometaphase chromosome and immunological studies in different derivatives of balanced t(8;14)(p231;q323).

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 276, doi. 10.1111/j.1399-0004.1984.tb04394.x

By:

Tranebjærg, Lisbeth;
Mansa, Bendt;
Steenbuch, Lise

Publication type:

Article

Experience with transabdominal fine needle biopsy from chorionic villi in the first trimester: an alternative to amniocentesis.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 272, doi. 10.1111/j.1399-0004.1984.tb04392.x

By:

Smidt-Jensen', S.;
Hahnemann', N.;
Jensen, P. K. A.;
Therkelsen, A. J.

Publication type:

Article

Hereditary lymphedema: a new combination of symptoms not fitting into present classifications.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 254, doi. 10.1111/j.1399-0004.1984.tb04383.x

By:

Kääriäinen, Helena

Publication type:

Article

Four cases of the prenatal diagnosis of trisomy 20 mosaicism with a follow up investigation.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 265, doi. 10.1111/j.1399-0004.1984.tb04388.x

By:

Møllekær, A. M.;
Jensen, P. K. A.;
Friedrich, U.;
Bruun-Petersen, G.

Publication type:

Article

Familial porencephaly.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 236, doi. 10.1111/j.1399-0004.1984.tb04375.x

By:

Airaksinen, Eila M.

Publication type:

Article

FamiIial vascuIar malformations Report of 25 members of one family.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 221, doi. 10.1111/j.1399-0004.1984.tb04371.x

By:

Pasyk, Krystyna A.;
Argenta, Louis C.;
Erickson, Robert P.

Publication type:

Article

Distal trisomy 14q syndrome; a case report.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 231, doi. 10.1111/j.1399-0004.1984.tb04373.x

By:

Markkanen, Anne;
Somer, Mirja;
Nordström, Ann-Marie

Publication type:

Article

Two cases of 11p13 interstitial deletion and unusual clinical features.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 247, doi. 10.1111/j.1399-0004.1984.tb04380.x

By:

Gustavson, K.-H.;
Annerén, G.;
Wranne, L.

Publication type:

Article

The Occurrence of 'Finnish' hereditary diseases in the other Nordic countries.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 269, doi. 10.1111/j.1399-0004.1984.tb04390.x

By:

Norio, Reijo

Publication type:

Article

Cholesterol ester storage disease in an adult presenting with sea-blue histiocytosis.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 195, doi. 10.1111/j.1399-0004.1984.tb04367.x

By:

Besley, G. T. N.;
Broadhead, D. M.;
Lawlor, Emer;
McCann, S. R.;
Dempsey, J. D.;
Drury, M. I.;
Crowe, J.

Publication type:

Article

Unexpected findings at prenatal diagnosis.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 268, doi. 10.1111/j.1399-0004.1984.tb04389.x

By:

Møller, Pål;
Hagen, Carl Birger;
Berg, Kåre;
Ormerod, Eli

Publication type:

Article

Rocker bottom feet.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 258, doi. 10.1111/j.1399-0004.1984.tb04385.x

By:

Lyngbye, Troels;
Møllekær, Anne M.

Publication type:

Article

Autosomal recesslve ichthyosis in Norway: II. Sjøgren-Larsson-like ichthyosis without CNS or eye involvement.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 242, doi. 10.1111/j.1399-0004.1984.tb04378.x

By:

Gedde-Dahl, T.;
Rajka, G.;
Larsen, T. Eeg;
Jellum, E.

Publication type:

Article

Papers presented at The Third Nordic Conference of Medical Genetics Helsinki, Finland, 17-19 February 1984.

Published in:: Clinical Genetics, 1984, v. 26, n. 3, p. 235, doi. 10.1111/j.1399-0004.1984.tb04374.x
Publication type:: Article

Nager's acrofacial dysostosis with thumb duplication: report of a case.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 228, doi. 10.1111/j.1399-0004.1984.tb04372.x

By:

Giugliani, Roberto;
Pereira, Carmen Heller

Publication type:

Article

Basement membrane proteins in human amniotic fluid.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 271, doi. 10.1111/j.1399-0004.1984.tb04391.x

By:

Risteli, Leila;
Autio-Harmainen, Helena;
Koskull, Harriet;
Risteli, Juha

Publication type:

Article

Ankylosing spondylitis is part of a multifactorial syndrome: hereditary multifocal relapsing inflammation (HEMRI).

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 187, doi. 10.1111/j.1399-0004.1984.tb04366.x

By:

Møllerand, Pål;
Berg, Kare

Publication type:

Article

Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 169, doi. 10.1111/j.1399-0004.1984.tb04363.x

By:

Hecht, Frederick;
Hecht, Barbara K.

Publication type:

Article

A 5p;22q reciprocal translocation with a high risk for segregation of unbalanced offspring.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 252, doi. 10.1111/j.1399-0004.1984.tb04382.x

By:

Jensen, P. K. A.

Publication type:

Article

First trimester biopsies of chorionic villi for prenatal diagnosis: experience of two laboratories.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 263, doi. 10.1111/j.1399-0004.1984.tb04387.x

By:

Mikkelsen, M.;
Søndergaard, F.;
Tønnesen, T.;
Marsk, L.;
Lindsten, J.

Publication type:

Article

Scoliosis and retinal changes in a G syndrome carrier.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 274, doi. 10.1111/j.1399-0004.1984.tb04393.x

By:

Somer, Mirja;
Westerlund, Antero

Publication type:

Article

Prader-Willi syndrome in a child with a balanced (X;15) de novo translocation.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 245, doi. 10.1111/j.1399-0004.1984.tb04379.x

By:

Gustavson, Karl-Henrik;
Annerén, Göran;
Jagell, Sten

Publication type:

Article

Occurrences of methylmalonic aciduria and Hartnup disorder in the same family.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 216, doi. 10.1111/j.1399-0004.1984.tb04370.x

By:

Shih, V. E.;
Coulombe, J. T.;
Wadman, S. K.;
Duran, M.;
Waelkens, J. J. J.

Publication type:

Article

Alpers' disease.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 256, doi. 10.1111/j.1399-0004.1984.tb04384.x

By:

Lyngbye, Troels;
Kristensen, Hella Koopmann;
Bojsen-Møller, Marie

Publication type:

Article

Hydrops fetalis: a new aspect of trisomy 18.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 238, doi. 10.1111/j.1399-0004.1984.tb04376.x

By:

Fisker, P.;
Smidt-Jensen, S.

Publication type:

Article

Meningocele in a boy with trisomy 13.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 278, doi. 10.1111/j.1399-0004.1984.tb04395.x

By:

ØRstavik, K. H.;
Hagen, C. B.;
Lindemann, R.;
Sande, H. A.;
Strøm, E. H.

Publication type:

Article

Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333).

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 209, doi. 10.1111/j.1399-0004.1984.tb04369.x

By:

Beemer, F. A.;
France, H. F. de;
Rosina-Angelista, I. J. M.;
Gerards, L. J.;
Cats, B. P.;
Guyt, R.

Publication type:

Article

Semi-lethal bone dysplasia in three sibs: a new genetic disorder.

Published in:

Clinical Genetics, 1984, v. 26, n. 3, p. 249, doi. 10.1111/j.1399-0004.1984.tb04381.x

By:

Holmgren, G.;
Forsell, Å.;
Kääriäinen, H.;
Maroteaux, P.

Publication type:

Article