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First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.
Guterman, Sarah; Hervé, Bérénice; Rivière, Julie; Fauvert, Delphine; Clement, Patrice; Vialard, François.
Affiliation
  • Guterman S; EA7404-GIG, University Simone Veil of Health Sciences, UVSQ, Montigny le Bretonneux, France.
  • Hervé B; EA7404-GIG, University Simone Veil of Health Sciences, UVSQ, Montigny le Bretonneux, France.
  • Rivière J; Cytogenetics Laboratory, Poissy/St Germain Hospital, Poissy, France.
  • Fauvert D; Lilas Hospital, Les Lilas, France.
  • Clement P; Cytogenetics Laboratory, Poissy/St Germain Hospital, Poissy, France.
  • Vialard F; Clement Laboratory, Le Blanc-Mesnil, France.
J Obstet Gynaecol Res ; 44(3): 570-575, 2018 Mar.
Article in En | MEDLINE | ID: mdl-29160022
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prenatal Diagnosis / Craniofacial Abnormalities / Fetal Diseases / Heart Defects, Congenital / Intellectual Disability Type of study: Diagnostic_studies / Systematic_reviews Limits: Adult / Female / Humans / Pregnancy Language: En Journal: J Obstet Gynaecol Res Journal subject: GINECOLOGIA / OBSTETRICIA Year: 2018 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prenatal Diagnosis / Craniofacial Abnormalities / Fetal Diseases / Heart Defects, Congenital / Intellectual Disability Type of study: Diagnostic_studies / Systematic_reviews Limits: Adult / Female / Humans / Pregnancy Language: En Journal: J Obstet Gynaecol Res Journal subject: GINECOLOGIA / OBSTETRICIA Year: 2018 Document type: Article Affiliation country: Country of publication: