All individuals with variants in gene UQCRC2

6 entries on 1 page. Showing entries 1 - 6.
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00000269 23281071-Fam PubMed: Miyake 2013, Journal: Miyake 2013 6-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents/relatives F;M yes Mexico - - - - - MC3DN see paper; ... 1 3 Noriko Miyake
00050458 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, intrauterine growth retardation, global developmental delay, abnormal size of the palpebral fissures, prominent nose, short 4th metacarpal, clinodactyly of the 5th finger, cutaneous syndactyly of toes, aggressive behavior 1 1 Johan den Dunnen
00050478 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) F - United Kingdom (Great Britain) - - - Decipher - ? synophrys, early onset of puberty, persistence of primary teeth, specific learning disability, preauricular skin tag, epicanthus, hypertelorism, dental crowding 1 2 Johan den Dunnen
00050660 - PubMed: DDDS 2015, Journal: DDDS 2015,PubMed: Faundes 2018 affected, unknown family members M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, microcephaly, clinodactyly of the 5th finger, short nose 1 1 Johan den Dunnen
00165321 28275242-Pat PubMed: Gaignard 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents - - France - - - - - MC3DN see paper; …, neonatal lactic acidosis, hypoglycemia, severe episodes of liver failure 1 3 Johan den Dunnen
00291422 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 61 Mohammed Faruq
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