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Identification of a 6-month-old baby with a combination of WAGR and Potocki-Shaffer contiguous deletion syndromes by SNP array testing.
Meng, Yan; Yang, Jun; Tian, Chan; Qiao, Jie.
Affiliation
  • Meng Y; Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China.
  • Yang J; National Clinical Research Center for Obstetrics and Gynecology, Beijing, 100191, China.
  • Tian C; Key Laboratory of Assisted Reproduction (Peking University), Ministry of Education, Beijing, 100191, China.
  • Qiao J; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing, 100191, China.
Hereditas ; 157(1): 23, 2020 May 23.
Article de En | MEDLINE | ID: mdl-32446308
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie des exostoses multiples / Syndrome WAGR / Maladies chromosomiques Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Female / Humans / Infant Langue: En Journal: Hereditas Année: 2020 Type de document: Article Pays d'affiliation: Chine Pays de publication: Royaume-Uni
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie des exostoses multiples / Syndrome WAGR / Maladies chromosomiques Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Female / Humans / Infant Langue: En Journal: Hereditas Année: 2020 Type de document: Article Pays d'affiliation: Chine Pays de publication: Royaume-Uni