Intragenic tetranucleotide repeat polymorphism at the human histidase (HAL) locus.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 194, doi. 10.1111/j.1399-0004.1997.tb02545.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1997 AND VI 52 AND IP 3
Results: 14
1
2
Expand Long PCR for fragile X mutation detection.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 147, doi. 10.1111/j.1399-0004.1997.tb02535.x
- By:
- Publication type:
- Article
3
Turner syndrome in a mother and daughter: r(X) and fertility.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 187, doi. 10.1111/j.1399-0004.1997.tb02543.x
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- Publication type:
- Article
4
Consanguineous marriage and its clinical consequences in migrants to Australia.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 142, doi. 10.1111/j.1399-0004.1997.tb02534.x
- By:
- Publication type:
- Article
5
A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 135, doi. 10.1111/j.1399-0004.1997.tb02533.x
- By:
- Publication type:
- Article
6
A bi-allelic tetranucleotide repeat in the promoter of the human inducible nitric oxide synthase gene.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 192, doi. 10.1111/j.1399-0004.1997.tb02544.x
- By:
- Publication type:
- Article
7
Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 196, doi. 10.1111/j.1399-0004.1997.tb02546.x
- By:
- Publication type:
- Article
8
Influence of APOH protein polymorphism on apoH levels in normal and diabetic subjects.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 167, doi. 10.1111/j.1399-0004.1997.tb02538.x
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- Publication type:
- Article
9
Familial inv(X)(p22q22): ovarian dysgenesis in two sisters with del Xq and fertility in one male carrier.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 180, doi. 10.1111/j.1399-0004.1997.tb02541.x
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- Publication type:
- Article
10
Differences in the prevalence of a TaqI RFLP in the 3' flanking region of the α.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 162, doi. 10.1111/j.1399-0004.1997.tb02537.x
- By:
- Publication type:
- Article
11
A case of de novo interstitial deletion of chromosome 5(q33q34).
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 173, doi. 10.1111/j.1399-0004.1997.tb02539.x
- By:
- Publication type:
- Article
12
Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 184, doi. 10.1111/j.1399-0004.1997.tb02542.x
- By:
- Publication type:
- Article
13
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies.
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 155, doi. 10.1111/j.1399-0004.1997.tb02536.x
- By:
- Publication type:
- Article
14
An additional case of craniodigital syndrome: variable expression of the Filippi syndrome?
- Published in:
- Clinical Genetics, 1997, v. 52, n. 3, p. 177, doi. 10.1111/j.1399-0004.1997.tb02540.x
- By:
- Publication type:
- Article