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3. Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder. de Munnik SA; Otten BJ; Schoots J; Bicknell LS; Aftimos S; Al-Aama JY; van Bever Y; Bober MB; Borm GF; Clayton-Smith J; Deal CL; Edrees AY; Feingold M; Fryer A; van Hagen JM; Hennekam RC; Jansweijer MC; Johnson D; Kant SG; Opitz JM; Ramadevi AR; Reardon W; Ross A; Sarda P; Schrander-Stumpel CT; Sluiter AE; Temple IK; Terhal PA; Toutain A; Wise CA; Wright M; Skidmore DL; Samuels ME; Hoefsloot LH; Knoers NV; Brunner HG; Jackson AP; Bongers EM Am J Med Genet A; 2012 Nov; 158A(11):2733-42. PubMed ID: 23023959 [TBL] [Abstract][Full Text] [Related]
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6. Further insight into the phenotype associated with a mutation in the ORC6 gene, causing Meier-Gorlin syndrome 3. Shalev SA; Khayat M; Etty DS; Elpeleg O Am J Med Genet A; 2015 Mar; 167A(3):607-11. PubMed ID: 25691413 [TBL] [Abstract][Full Text] [Related]
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20. Meier-Gorlin syndrome caused by ORC1 mutation associated with chromosomal breakage - coincidental finding or new feature of known syndrome? Vojtková J; Čiljaková M; Jeseňák M; Bánovčin P Endokrynol Pol; 2019; 70(5):457-459. PubMed ID: 31274184 [No Abstract] [Full Text] [Related] [Next] [New Search]