All individuals with variants in gene MEA1

6 entries on 1 page. Showing entries 1 - 6.
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AscendingIndividual ID     

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Owner     
00050375 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? severe intellectual disability, hydrocephalus, chronic diarrhea, hypoglycemia 1 1 Johan den Dunnen
00050506 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, seizures, ventriculomegaly, narrow forehead, downslanted palpebral fissures, pyloric stenosis, narrow palate, generalized hypotonia, macrocephaly, ventriculomegaly 1 1 Johan den Dunnen
00050643 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, congenital muscular torticollis, congenital hip dislocation 1 1 Johan den Dunnen
00050675 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, deeply set eye, abnormality of vision, myopia, strabismus, generalized hypotonia 1 1 Johan den Dunnen
00080819 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - HJS1;MRD35 Mental retardation, autosomal dominant 35 (OMIM:616355) 1 1 Daniel Trujillano
00208599 Fam301 - - - - - - - - - - cancer, colon - 1 3 Xiang Jiao
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