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Monosomy 18p.
Turleau, Catherine.
Affiliation
  • Turleau C; Cytogénétique AP-HP et Inserm U781, Université Paris Descartes, Hôpital Necker-Enfants Malades, 75015 Paris, France. turleau@necker.fr
Orphanet J Rare Dis ; 3: 4, 2008 Feb 19.
Article in En | MEDLINE | ID: mdl-18284672
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 18 / Chromosome Disorders / Monosomy Type of study: Diagnostic_studies / Incidence_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2008 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 18 / Chromosome Disorders / Monosomy Type of study: Diagnostic_studies / Incidence_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2008 Document type: Article Affiliation country: