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Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability

European Journal of Human Genetics - United Kingdom
doi 10.1038/s41431-018-0281-5
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Abstract

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Categories
Genetics
Date

October 5, 2018

Authors
Rosalind VerheijeGabriel S. KupchikBertrand IsidorHester Y. KroesSally Ann LynchLara HawkesMaja HempelBruce D. GelbJamal GhoumidGuylaine D’AmoursKate ChandlerChristèle DubourgSara LoddoZeynep TümerCharles Shaw-SmithMathilde NizonMichael ShevellEvelien Van HoofKwame Anyane-YeboaGaetana CerboneJill Clayton-SmithBenjamin CognéPierre CorreAnniek CorveleynMarie De BorreTina Duelund HjortshøjMélanie FradinMarc GewilligElizabeth GoldmuntzGreet HensEmmanuelle LemyreHubert JournelUsha KiniFanny KortümCedric Le CaignecAntonio NovelliSylvie OdentFlorence PetitAnya Revah-PolitiNicholas StongTim M. StromEllen van BinsbergenKoenraad DevriendtJeroen Breckpot
Publisher

Springer Science and Business Media LLC

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