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https://pubmed.ncbi.nlm.nih.gov/3789005/

New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous...

Eight patients (4 males, 4 females) were affected with a previously undefined multiple congenital anomalies/mental retardation syndrome which was designated...

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https://pubmed.ncbi.nlm.nih.gov/8673085/

Identification of the gene FMR2, associated with FRAXE mental retardation

Five folate-sensitive fragile sites have been characterized at the molecular level (FRAXA, FRAXE, FRAXF, FRA16A and FRA11B). Three of them (FRAXA, FRAXE and...

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https://pubmed.ncbi.nlm.nih.gov/35598272/

[Clinical and genetic analysis of a child with mental retardation autosomal dominant 7]

The exon11: c.1920_c.1927delCCTCTACC (p.Ser641Rfs*31) mutation in DYRK1A gene was the genetic etiology of the case, which enriches the pathogenic gene spectrum...

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https://ojp.gov/ncjrs/virtual-library/abstracts/mental-retardation-training-key

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https://www.semanticscholar.org/topic/Profound-Mental-Retardation/443867

Profound Mental Retardation | Semantic Scholar

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