Deletion of the short arm of chromosome 20.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 140, doi. 10.1111/j.1399-0004.1988.tb03425.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1988 AND VI 33 AND IP 2
Results: 18
1
2
Clinical findings in 12 patients with MPS IV A (Morquio's disease).
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 111, doi. 10.1111/j.1399-0004.1988.tb03421.x
- By:
- Publication type:
- Article
3
Announcements.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 144, doi. 10.1111/j.1399-0004.1988.tb03428.x
- Publication type:
- Article
4
Clinical findings in 12 patients with MPS IV A (Morquio's disease).
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 126, doi. 10.1111/j.1399-0004.1988.tb03423.x
- By:
- Publication type:
- Article
5
Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 108, doi. 10.1111/j.1399-0004.1988.tb03420.x
- By:
- Publication type:
- Article
6
Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 78, doi. 10.1111/j.1399-0004.1988.tb03414.x
- By:
- Publication type:
- Article
7
Clinical findings in 12 patients with MPS IV A (Morquio's disease).
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 121, doi. 10.1111/j.1399-0004.1988.tb03422.x
- By:
- Publication type:
- Article
8
X-linked retinoschisis and linkage.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 143, doi. 10.1111/j.1399-0004.1988.tb03427.x
- By:
- Publication type:
- Article
9
A new rare heritable fragile site at 8q24.1 found in a Japanese population.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 91, doi. 10.1111/j.1399-0004.1988.tb03417.x
- By:
- Publication type:
- Article
10
Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 73, doi. 10.1111/j.1399-0004.1988.tb03413.x
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- Publication type:
- Article
11
A patient with an interstitial deletion of the short arm of chromosome 6.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 95, doi. 10.1111/j.1399-0004.1988.tb03418.x
- By:
- Publication type:
- Article
12
Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 131, doi. 10.1111/j.1399-0004.1988.tb03424.x
- By:
- Publication type:
- Article
13
Variability gene effect on cholesterol at the Kidd blood group locus.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 102, doi. 10.1111/j.1399-0004.1988.tb03419.x
- By:
- Publication type:
- Article
14
Translocation t(13;14) in nine generations with a case of translocation homozygosity.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 83, doi. 10.1111/j.1399-0004.1988.tb03415.x
- By:
- Publication type:
- Article
15
A de novo interstitial deletion of chromosome 6 (q22.2q23.1).
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 65, doi. 10.1111/j.1399-0004.1988.tb03411.x
- By:
- Publication type:
- Article
16
Male transmission of Apert syndrome.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 87, doi. 10.1111/j.1399-0004.1988.tb03416.x
- By:
- Publication type:
- Article
17
EEC syndrome sine sine?
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 69, doi. 10.1111/j.1399-0004.1988.tb03412.x
- By:
- Publication type:
- Article
18
Oro-facial-digital syndrome II.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 141, doi. 10.1111/j.1399-0004.1988.tb03426.x
- By:
- Publication type:
- Article