Maternally inherited hearing impairment.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 409, doi. 10.1034/j.1399-0004.2000.570601.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2000 AND VI 57 AND IP 6
Results: 14
1
2
Interacting proteins in yeast – a perfect marriage.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 416, doi. 10.1034/j.1399-0004.2000.570602.1.x
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- Publication type:
- Article
3
A genetic screen for suppression of polyglutamine induced toxicity in flies.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 418, doi. 10.1034/j.1399-0004.2000.570602.2.x
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- Publication type:
- Article
4
Expression profiling in cancer using gene chips.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 415, doi. 10.1034/j.1399-0004.2000.570602.x
- By:
- Publication type:
- Article
5
Genetic landmarks through philately – Jean Martin Charcot (1825–1893) and Charcot–Marie–Tooth disease.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 420, doi. 10.1034/j.1399-0004.2000.570603.x
- By:
- Publication type:
- Article
6
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 423, doi. 10.1034/j.1399-0004.2000.570604.x
- By:
- Publication type:
- Article
7
MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis?
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 430, doi. 10.1034/j.1399-0004.2000.570605.x
- By:
- Publication type:
- Article
8
Hypogonadotrophic hypogonadism in Roifman syndrome.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 435, doi. 10.1034/j.1399-0004.2000.570606.x
- By:
- Publication type:
- Article
9
Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 439, doi. 10.1034/j.1399-0004.2000.570607.x
- By:
- Publication type:
- Article
10
Vertebral anomalies in a new family with ODED syndrome.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 444, doi. 10.1034/j.1399-0004.2000.570608.x
- By:
- Publication type:
- Article
11
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri–Weill dyschondrosteosis.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 449, doi. 10.1034/j.1399-0004.2000.570609.x
- By:
- Publication type:
- Article
12
Hemochromatosis in Galicia (NW Spain): a Celtic influence?
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 454, doi. 10.1034/j.1399-0004.2000.570610.x
- By:
- Publication type:
- Article
13
The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 456, doi. 10.1034/j.1399-0004.2000.570611.x
- By:
- Publication type:
- Article
14
Psychomotor development in Cri du Chat Syndrome.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 6, p. 459, doi. 10.1034/j.1399-0004.2000.570612.x
- By:
- Publication type:
- Article