A rare rearrangement of 5q31.2 in a child with a neurodevelopmental syndrome.

Goldenstein, Hagit; Shrem, Sara Beni; Weiss, Omri; Zeligson, Sharon; Segel, Reeval; Mory, Adi; Weiss, Karin

Goldenstein, Hagit; Shrem, Sara Beni; Weiss, Omri; Zeligson, Sharon; Segel, Reeval; Mory, Adi; Weiss, Karin.

Afiliación

Goldenstein H; The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa.
Shrem SB; Pediatric Neurodevelopment Service, Meuchedet Health Services.
Weiss O; Medical Genetics Institute, Shaare Zedek Medical Center and Hebrew University-Hadassah School of Medicine, Jerusalem.
Zeligson S; Medical Genetics Institute, Shaare Zedek Medical Center and Hebrew University-Hadassah School of Medicine, Jerusalem.
Segel R; Medical Genetics Institute, Shaare Zedek Medical Center and Hebrew University-Hadassah School of Medicine, Jerusalem.
Mory A; The Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
Weiss K; The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa.

Clin Dysmorphol ; 30(4): 181-185, 2021 Oct 01.

Article en En | MEDLINE | ID: mdl-34232135

Asunto(s)

Aberraciones Cromosómicas; Deleción Cromosómica; Niño; Cromosomas Humanos Par 5/genética; Humanos; Síndrome

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas / Deleción Cromosómica Límite: Child / Humans Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 2021 Tipo del documento: Article

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