Häufiges Syndrom, selten diagnostiziert: das Triple-X-Syndrom

Author:

Schwemmle C.,Ptok M.

Publisher

Springer Science and Business Media LLC

Subject

Surgery,Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Chiappedi M, Vincenzi S de, Dolci R et al (2011) Gilles de la Tourette’s syndrome in a patient with 47(XXX) syndrome: a case report. J Med Case Rep 5:542

2. Guichet A, Briault S, Moraine C, Turleau C (2004) Trisomy X. ACLF (Association des Cytogeneticiens de Langue Francais) retrospective study. Ann Genet 39:117–122

3. Haverty CE, Lin AE, Simpson E et al (2004) 47,XXX associated with malformations. Am J Med Genet A 125:108–111

4. Hook EB (1983) Chromosome abnormalities and spontaneous fetal death following amniocentesis: further data and associations with maternal age. Am J Hum Genet 35:110–116

5. Hook E (1992) Chromosome abnormalities: prevalence, risks and recurrence. In: Brock DJH, Rodeck CH, Ferguson-Smith MA (Hrsg) Prenatal diagnosis and screening. Churchill Livingstone, Edinburgh London New York, S 351–392

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