Short Report on DNA Marker at Candidate Locus.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 106, doi. 10.1111/j.1399-0004.1996.tb02359.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1996 AND VI 50 AND IP 2
Results: 14
1
2
Poland sequence in two siblings suggesting an autosomal inheritance transmission.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 93, doi. 10.1111/j.1399-0004.1996.tb02355.x
- By:
- Publication type:
- Article
3
Multifactorial inheritance of non-syndromic macrocephaly.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 57, doi. 10.1111/j.1399-0004.1996.tb02349.x
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- Publication type:
- Article
4
Osteopenia, abnormal dentition, hydrops fetalis and communicating hydrocephalus: unusual early clinical signs in Coffin-Lowry syndrome.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 112, doi. 10.1111/j.1399-0004.1996.tb02362.x
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- Publication type:
- Article
5
Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12 → q13.3) inherited from the mother.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 63, doi. 10.1111/j.1399-0004.1996.tb02350.x
- By:
- Publication type:
- Article
6
Midline congenital anomalies: the estimated occurrence among American Indian and Alaska Native infants.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 74, doi. 10.1111/j.1399-0004.1996.tb02351.x
- By:
- Publication type:
- Article
7
Medical Ethics:The right not to know-worthy of preservation any longer? An ethical perspective.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 85, doi. 10.1111/j.1399-0004.1996.tb02353.x
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- Publication type:
- Article
8
De novo direct duplication 3 (p25→pter): a previously undescribed chromosomal aberration.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 96, doi. 10.1111/j.1399-0004.1996.tb02356.x
- By:
- Publication type:
- Article
9
The molecular characterization of Gaucher disease in South Africa.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 78, doi. 10.1111/j.1399-0004.1996.tb02352.x
- By:
- Publication type:
- Article
10
Exclusion of Treacher Collins Franceschetti syndrome in a subject with tetralogy of Fallot and cryptorchidism.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 89, doi. 10.1111/j.1399-0004.1996.tb02354.x
- By:
- Publication type:
- Article
11
Short Report on DNA Marker at Candidate Locus.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 108, doi. 10.1111/j.1399-0004.1996.tb02360.x
- By:
- Publication type:
- Article
12
Exceptions to the rule: individuals with FAP specific CHRPE and mutations in exon 6 of the APC gene.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 110, doi. 10.1111/j.1399-0004.1996.tb02361.x
- By:
- Publication type:
- Article
13
The evaluation of gonosomal mosaics: lymphocyte interphase nuclei analyzed by FISH.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 99, doi. 10.1111/j.1399-0004.1996.tb02357.x
- By:
- Publication type:
- Article
14
Molecular characterization of 21p-variant chromosome.
- Published in:
- Clinical Genetics, 1996, v. 50, n. 2, p. 103, doi. 10.1111/j.1399-0004.1996.tb02358.x
- By:
- Publication type:
- Article