All individuals with variants in gene MAOA

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

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Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

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Owner     
00050524 - PubMed: DDDS 2015, Journal: DDDS 2015 affected, unknown family members F - United Kingdom (Great Britain) - - 0 Decipher - ? pontocerebellar hypoplasia, progressive microcephaly, cortical visual impairment, severe global developmental delay 1 1 Johan den Dunnen
00111408 S_114 PubMed: Popp 2017, Journal: Popp 2017 - M no ? (unknown) - - 0 - - BRNRS Male, 7 y, speech delay, moderate ID, behavioral anomalies (maternal XI 82%) 1 1 Bernt Popp
00172292 19377476-Pat? PubMed: Tarpey 2009 - M - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 64 Lucy Raymond
00172293 19377476-Pat? PubMed: Tarpey 2009 - M - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 10 Lucy Raymond
00172294 19377476-Pat? PubMed: Tarpey 2009 - M - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 101 Lucy Raymond
00296779 APN-16 PubMed: Redin 2014 analysis 106 patients M - France - - 0 - - ID borderline intellectual disability 1 1 Johan den Dunnen
00307751 UK10K_FINDWGA5411323 PubMed: Grozeva 2015, Journal: Grozeva 2015 - M - - - - 0 - - ID - 1 1 Johan den Dunnen
00334962 H1 PubMed: Jin 2017 - - - China - - 0 - - ? see paper; ... 1 1 LOVD
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