18p monosomy with GH-deficiency and empty sella: good response to GH-treatment.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 254, doi. 10.1111/j.1399-0004.1995.tb04306.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1995 AND VI 47 AND IP 5
Results: 13
1
2
Increased and decreased relative risk for noninsulin-dependent diabetes mellitus conferred by HLA class II and by CD4 alleles.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 225, doi. 10.1111/j.1399-0004.1995.tb04301.x
- By:
- Publication type:
- Article
3
Evidence for genetic influences on smoking in adult women twins.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 236, doi. 10.1111/j.1399-0004.1995.tb04303.x
- By:
- Publication type:
- Article
4
Haspeslagh syndrome without severe mental retardation and pterygia?
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 263, doi. 10.1111/j.1399-0004.1995.tb04308.x
- By:
- Publication type:
- Article
5
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 248, doi. 10.1111/j.1399-0004.1995.tb04305.x
- By:
- Publication type:
- Article
6
A Taql RFLP in the type IV collagen α5 chain gene (COL4A5) with the rare allele more frequently found in seven Chinese Alport syndrome patients.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 278, doi. 10.1111/j.1399-0004.1995.tb04313.x
- By:
- Publication type:
- Article
7
A highly informative BamHI RFLP in the type IV collagen α5 chain gene (COL4A5).
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 276, doi. 10.1111/j.1399-0004.1995.tb04312.x
- By:
- Publication type:
- Article
8
Partial deletion 11q: report of a case with a large terminal deletion 11q21-qter without loss of telomeric sequences, and review of the literature.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 231, doi. 10.1111/j.1399-0004.1995.tb04302.x
- By:
- Publication type:
- Article
9
Clinical overlap of Beckwith-Wiedemann, Perlman and Simpson-Golabi-Behmel syndromes: a diagnostic pitfall.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 257, doi. 10.1111/j.1399-0004.1995.tb04307.x
- By:
- Publication type:
- Article
10
A small supernumerary marker chromosome X identified by in situ hybridization.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 270, doi. 10.1111/j.1399-0004.1995.tb04310.x
- By:
- Publication type:
- Article
11
A simple method to detect the RYR1 mutation G1021A, a cause of malignant hyperthermia susceptibility.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 274, doi. 10.1111/j.1399-0004.1995.tb04311.x
- By:
- Publication type:
- Article
12
Familial intestinal polyatresia syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 245, doi. 10.1111/j.1399-0004.1995.tb04304.x
- By:
- Publication type:
- Article
13
Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome?
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 267, doi. 10.1111/j.1399-0004.1995.tb04309.x
- By:
- Publication type:
- Article