Works matching IS 00099163 AND DT 1989 AND VI 36 AND IP 6
Results: 9
3C syndrome: another case.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 465, doi. 10.1111/j.1399-0004.1989.tb03380.x
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- Article
A complex deformity of appendicular skeleton and shoulder with congenital heart disease in three generations of a Jordanian family.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 442, doi. 10.1111/j.1399-0004.1989.tb03374.x
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- Article
Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 464, doi. 10.1111/j.1399-0004.1989.tb03379.x
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- Article
Hereditary spastic diplegia with mental retardation in two young siblings.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 439, doi. 10.1111/j.1399-0004.1989.tb03373.x
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- Publication type:
- Article
High incidence of Bardet Biedl syndrome among the Bedouin.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 463, doi. 10.1111/j.1399-0004.1989.tb03378.x
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- Publication type:
- Article
Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive condition.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 456, doi. 10.1111/j.1399-0004.1989.tb03376.x
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- Publication type:
- Article
An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 451, doi. 10.1111/j.1399-0004.1989.tb03375.x
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- Publication type:
- Article
Announcements.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 466, doi. 10.1111/j.1399-0004.1989.tb03381.x
- Publication type:
- Article
Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 459, doi. 10.1111/j.1399-0004.1989.tb03377.x
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- Publication type:
- Article