8q22-->qter duplication in a child with multiple congenital malformations: case report.

Sasiadek, M; Stembalska, A; Schlade, K; Zych, M

Sasiadek, M; Stembalska, A; Schlade, K; Zych, M.

Affiliation

Sasiadek M; Department of Genetics, Department of Pathophysiology, Wroclaw University of Medicine. sasiadek@gen.am.wroc.pl

Med Sci Monit ; 6(1): 141-4, 2000.

Article in En | MEDLINE | ID: mdl-11208302

Subject(s)

Abnormalities, Multiple/genetics; Chromosome Aberrations; Chromosomes, Human, Pair 8/genetics; Translocation, Genetic; Abnormalities, Multiple/pathology; Chromosomes, Human, Pair 14/genetics; Facial Bones/abnormalities; Female; Genitalia, Male/abnormalities; Humans; Infant; Karyotyping; Male; Pedigree

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Abnormalities, Multiple / Chromosomes, Human, Pair 8 / Chromosome Aberrations Limits: Female / Humans / Infant / Male Language: En Journal: Med Sci Monit Journal subject: MEDICINA Year: 2000 Document type: Article Country of publication: United States

Search on Google

Add to My VHL

XML

PubMed Links