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Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature.
Seto, Mimi Tin-Yan; Bertoli-Avella, Aida M; Cheung, Ka Wang; Chan, Kelvin Yuen-Kwong; Yeung, Kit San; Fung, Jasmine Lee-Fong; Beetz, Christian; Bauer, Peter; Luk, Ho Ming; Lo, Ivan Fai-Man; Lee, Chin Peng; Chung, Brian Hon-Yin; Kan, Anita Sik-Yau.
Afiliación
  • Seto MT; Department of Obstetrics and Gynecology, Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Bertoli-Avella AM; CENTOGENE GmbH, Rostock, Germany.
  • Cheung KW; Department of Obstetrics and Gynecology, Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Chan KY; Department of Obstetrics and Gynecology, Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Yeung KS; Prenatal Diagnostic Laboratory, Tsan Yuk Hospital, Sai Ying Pun, Hong Kong.
  • Fung JL; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Beetz C; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Bauer P; CENTOGENE GmbH, Rostock, Germany.
  • Luk HM; CENTOGENE GmbH, Rostock, Germany.
  • Lo IF; Department of Health, Clinical Genetic Service, Kowloon Bay, Hong Kong.
  • Lee CP; Department of Health, Clinical Genetic Service, Kowloon Bay, Hong Kong.
  • Chung BH; Department of Obstetrics and Gynecology, Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Kan AS; Department of Obstetrics and Gynecology, Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.
Am J Med Genet A ; 185(2): 384-389, 2021 02.
Article en En | MEDLINE | ID: mdl-33166031
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Discapacidades del Desarrollo / Proteínas de Transporte Vesicular / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Hong Kong
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Discapacidades del Desarrollo / Proteínas de Transporte Vesicular / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Hong Kong