Found: 7
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Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy.
- Published in:
- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 472, doi. 10.1111/j.1749-6632.1999.tb08614.x
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- Publication type:
- Article
Correlation of Abnormal Rapid FISH and Chromosome Results from Amniocytes for Prenatal Diagnosis.
- Published in:
- Fetal Diagnosis & Therapy, 2006, v. 21, n. 2, p. 235, doi. 10.1159/000089310
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- Publication type:
- Article
Trisomy 12 mosaicism in phenotypically normal fetuses following prenatal detection.
- Published in:
- 1990
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- Publication type:
- journal article
Schizophrenia susceptibility gene locus at Xp22.3.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 6, p. 455, doi. 10.1034/j.1399-0004.1999.550610.x
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- Publication type:
- Article
Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q.
- Published in:
- Clinical Genetics, 1995, v. 48, n. 3, p. 151, doi. 10.1111/j.1399-0004.1995.tb04076.x
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- Publication type:
- Article
Deletion of 15q12 in Angelman syndrome: report of 3 new cases.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 5, p. 229, doi. 10.1111/j.1399-0004.1992.tb03246.x
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- Publication type:
- Article
Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 5, p. 365, doi. 10.1111/j.1399-0004.1983.tb00087.x
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- Publication type:
- Article