2020
DOI: 10.1016/j.amsu.2020.10.063
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13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report

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“…It requires early diagnosis in cases of positive family history of Retinoblastoma [7], and screening should be considered for all family members and newborns of the affected individual [9]. Pregnancies in high-risk families require special attention, including antenatal ultrasonography and genetic testing [10].…”
Section: Introductionmentioning
confidence: 99%
“…It requires early diagnosis in cases of positive family history of Retinoblastoma [7], and screening should be considered for all family members and newborns of the affected individual [9]. Pregnancies in high-risk families require special attention, including antenatal ultrasonography and genetic testing [10].…”
Section: Introductionmentioning
confidence: 99%