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6. AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome. Laberthonnière C; Novoa-Del-Toro EM; Chevalier R; Broucqsault N; Rao VV; Trani JP; Nguyen K; Xue S; Reversade B; Robin JD; Baudot A; Magdinier F Biomedicines; 2021 Jun; 9(7):. PubMed ID: 34209568 [TBL] [Abstract][Full Text] [Related]
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16. Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2). Bodega B; Cardone MF; Müller S; Neusser M; Orzan F; Rossi E; Battaglioli E; Marozzi A; Riva P; Rocchi M; Meneveri R; Ginelli E BMC Evol Biol; 2007 Mar; 7():39. PubMed ID: 17359533 [TBL] [Abstract][Full Text] [Related]
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19. Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy. Tupler R; Berardinelli A; Barbierato L; Frants R; Hewitt JE; Lanzi G; Maraschio P; Tiepolo L J Med Genet; 1996 May; 33(5):366-70. PubMed ID: 8733044 [TBL] [Abstract][Full Text] [Related]
20. A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD). Winokur ST; Schutte B; Weiffenbach B; Washington SS; McElligott D; Chakravarti A; Wasmuth JH; Altherr MR Am J Hum Genet; 1993 Oct; 53(4):874-80. PubMed ID: 8213815 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]