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Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.
Gläser, Birgitta; Rossier, Eva; Barbi, Gotthold; Chiaie, Loredana Delle; Blank, Christian; Vogel, Walther; Kehrer-Sawatzki, Hildegard.
Affiliation
  • Gläser B; Department of Human Genetics, University of Ulm, Ulm, Germany.
Am J Med Genet A ; 116A(1): 66-70, 2003 Jan 01.
Article in En | MEDLINE | ID: mdl-12476454
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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 12 / Developmental Disabilities / Chromosome Deletion / Craniofacial Abnormalities Limits: Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2003 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 12 / Developmental Disabilities / Chromosome Deletion / Craniofacial Abnormalities Limits: Humans / Infant / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2003 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos