Works matching IS 00099163 AND DT 1989 AND VI 35 AND IP 4
Results: 15
Trisomy 5 mosaicism in amniotic fluid with normal outcome.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 282, doi. 10.1111/j.1399-0004.1989.tb02944.x
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- Article
Trisomy 9q3 syndrome: a case report and review of the literature.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 293, doi. 10.1111/j.1399-0004.1989.tb02947.x
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- Article
On the familial occurrence of congenital bilateral absence of vas deferens.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 268, doi. 10.1111/j.1399-0004.1989.tb02941.x
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Nonsyndromal microphthalmia.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 311, doi. 10.1111/j.1399-0004.1989.tb02950.x
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- Article
A 45,X/69,XXY fetus.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 285, doi. 10.1111/j.1399-0004.1989.tb02945.x
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- Article
A new case of deletion 1q42 syndrome.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 289, doi. 10.1111/j.1399-0004.1989.tb02946.x
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- Article
Dermatoglyphic features of a male with diploid/tetraploid mosaicism.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 310, doi. 10.1111/j.1399-0004.1989.tb02949.x
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- Article
Molecular deletions in the Duchenne/Becker muscular dystrophy gene.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 251, doi. 10.1111/j.1399-0004.1989.tb02939.x
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Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 233, doi. 10.1111/j.1399-0004.1989.tb02936.x
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- Article
Two other cases of ANOTHER syndrome? Family report and update.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 237, doi. 10.1111/j.1399-0004.1989.tb02937.x
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- Article
Prader-Willi Syndrome Scientific Conference III Abstracts.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 299, doi. 10.1111/j.1399-0004.1989.tb02948.x
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- Article
Brachydactyly type A-7 (Smorgasbord): a new entity.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 261, doi. 10.1111/j.1399-0004.1989.tb02940.x
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- Article
Sjögren-Larsson syndrome in Sweden: distribution of the gene.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 272, doi. 10.1111/j.1399-0004.1989.tb02942.x
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- Article
Variant nucleolus organizing regions and the risk of Down syndrome.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 243, doi. 10.1111/j.1399-0004.1989.tb02938.x
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- Article
An interstitial deletion of the long arm of chromosome 13.
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- Clinical Genetics, 1989, v. 35, n. 4, p. 276, doi. 10.1111/j.1399-0004.1989.tb02943.x
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- Article