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Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms.
Moradkhani, Kamran; Puechberty, Jacques; Blanchet, Patricia; Coubes, Christine; Lallaoui, Hakima; Lewin, Patricia; Lefort, Genevieve; Sarda, Pierre.
Affiliation
  • Moradkhani K; Department of Medical Genetics, Chu Montpellier, France.
Prenat Diagn ; 26(12): 1179-82, 2006 Dec.
Article in En | MEDLINE | ID: mdl-17075795
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Collection: 01-internacional Database: MEDLINE Main subject: Trisomy / Chromosomes, Human, Pair 16 / Chromosome Disorders / Mosaicism Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Pregnancy Language: En Journal: Prenat Diagn Year: 2006 Document type: Article Affiliation country: Francia Country of publication: Reino Unido
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Trisomy / Chromosomes, Human, Pair 16 / Chromosome Disorders / Mosaicism Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Pregnancy Language: En Journal: Prenat Diagn Year: 2006 Document type: Article Affiliation country: Francia Country of publication: Reino Unido