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001007385 001__ 1007385
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001007385 1001_ $$aPaul, Maimuna S.$$b0
001007385 245__ $$aA syndromic neurodevelopmental disorder caused by rare variants in PPFIA3$$honline, print
001007385 260__ $$aNew York, NY [u.a.]$$bCell Press$$c2024
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001007385 7001_ $$aMichener, Sydney L.$$b1
001007385 7001_ $$aPan, Hongling$$b2
001007385 7001_ $$aChan, Hiuling$$b3
001007385 7001_ $$aPfliger, Jessica M.$$b4
001007385 7001_ $$aRosenfeld, Jill A.$$b5
001007385 7001_ $$aLerma, Vanesa C.$$b6
001007385 7001_ $$aTran, Alyssa$$b7
001007385 7001_ $$aLongley, Megan A.$$b8
001007385 7001_ $$aLewis, Richard A.$$b9
001007385 7001_ $$aWeisz-Hubshman, Monika$$b10
001007385 7001_ $$aBekheirnia, Mir Reza$$b11
001007385 7001_ $$aBekheirnia, Nasim$$b12
001007385 7001_ $$aMassingham, Lauren$$b13
001007385 7001_ $$aZech, Michael$$b14
001007385 7001_ $$aWagner, Matias$$b15
001007385 7001_ $$aEngels, Hartmut$$b16
001007385 7001_ $$aCremer, Kirsten$$b17
001007385 7001_ $$aMangold, Elisabeth$$b18
001007385 7001_ $$aPeters, Sophia$$b19
001007385 7001_ $$aTrautmann, Jessica$$b20
001007385 7001_ $$aPerne, Claudia$$b21
001007385 7001_ $$aMester, Jessica L.$$b22
001007385 7001_ $$aGuillen Sacoto, Maria J.$$b23
001007385 7001_ $$aPerson, Richard$$b24
001007385 7001_ $$aMcDonnell, Pamela P.$$b25
001007385 7001_ $$aCohen, Stacey R.$$b26
001007385 7001_ $$aLusk, Laina$$b27
001007385 7001_ $$aCohen, Ana S. A.$$b28
001007385 7001_ $$aLe Pichon, Jean-Baptiste$$b29
001007385 7001_ $$aPastinen, Tomi$$b30
001007385 7001_ $$aZhou, Dihong$$b31
001007385 7001_ $$aEngleman, Kendra$$b32
001007385 7001_ $$aRacine, Caroline$$b33
001007385 7001_ $$aFaivre, Laurence$$b34
001007385 7001_ $$aMoutton, Sébastien$$b35
001007385 7001_ $$aDenommé-Pichon, Anne-Sophie$$b36
001007385 7001_ $$aKoh, Hyun Yong$$b37
001007385 7001_ $$aPoduri, Annapurna$$b38
001007385 7001_ $$aBolton, Jeffrey$$b39
001007385 7001_ $$0P:(DE-82)466582$$aKnopp, Cordula$$b40$$urwth
001007385 7001_ $$0P:(DE-82)1011582$$aJulia Suh, Dong Sun$$b41$$urwth
001007385 7001_ $$0P:(DE-82)006350$$aMaier, Andrea$$b42$$urwth
001007385 7001_ $$aToosi, Mehran Beiraghi$$b43
001007385 7001_ $$aKarimiani, Ehsan Ghayoor$$b44
001007385 7001_ $$aMaroofian, Reza$$b45
001007385 7001_ $$aSchaefer, Gerald Bradley$$b46
001007385 7001_ $$aRamakumaran, Vijayalakshmi$$b47
001007385 7001_ $$aVasudevan, Pradeep$$b48
001007385 7001_ $$aBanos-Pinero, Benito$$b49
001007385 7001_ $$aPagnamenta, Alistair T.$$b50
001007385 7001_ $$aPrasad, Chitra$$b51
001007385 7001_ $$aOsmond, Matthew$$b52
001007385 7001_ $$aSchuhmann, Sarah$$b53
001007385 7001_ $$aVasileiou, Georgia$$b54
001007385 7001_ $$aRuss-Hall, Sophie$$b55
001007385 7001_ $$aScheffer, Ingrid E.$$b56
001007385 7001_ $$aCarvill, Gemma L.$$b57
001007385 7001_ $$aMefford, Heather$$b58
001007385 7001_ $$aUndiagnosed Diseases Network$$b59$$eCollaboration author
001007385 7001_ $$aBacino, Carlos A.$$b60
001007385 7001_ $$aLee, Brendan H.$$b61
001007385 7001_ $$aChao, Hsiao-Tuan$$b62$$eCorresponding author
001007385 773__ $$0PERI:(DE-600)1473813-2$$a10.1016/j.ajhg.2024.03.009$$n4$$p805-805$$tThe American journal of human genetics$$v111$$x1537-6605
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