Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.

Malan, Valérie; Gesny, R; Morichon-Delvallez, N; Aubry, M C; Benachi, A; Sanlaville, D; Turleau, C; Bonnefont, J P; Fekete-Nihoul, C; Vekemans, M

Malan, Valérie; Gesny, R; Morichon-Delvallez, N; Aubry, M C; Benachi, A; Sanlaville, D; Turleau, C; Bonnefont, J P; Fekete-Nihoul, C; Vekemans, M.

Affiliation

Malan V; Service de Cytogénétique, University René Descartes-Paris 5, Paris, France. valerie.malan@nck.aphp.fr

Hum Reprod ; 22(4): 1037-41, 2007 Apr.

Article in En | MEDLINE | ID: mdl-17272360

Subject(s)

Chromosomes, Human, X; Chromosomes, Human, Y; Prenatal Diagnosis; Alleles; Amniocentesis; Female; Genotype; Haploidy; Humans; Infant, Newborn; Karyotyping; Maternal Age; Phenotype; Polymorphism, Genetic; Treatment Outcome

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Collection: 01-internacional Database: MEDLINE Main subject: Prenatal Diagnosis / Chromosomes, Human, X / Chromosomes, Human, Y Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Newborn Language: En Journal: Hum Reprod Journal subject: MEDICINA REPRODUTIVA Year: 2007 Document type: Article Affiliation country: France

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