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Literature for OMIM 614897: HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16
Xenbase Articles:
( Denotes literature images)
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance., Schulz Y,Wehner P,Opitz L,Salinas-Riester G,Bongers EM,van Ravenswaaij-Arts CM,Wincent J,Schoumans J,Kohlhase J,Borchers A,Pauli S, Hum Genet. August 1, 2014; 133(8):1432-1203. |
Sema3a plays a role in the pathogenesis of CHARGE syndrome., Ufartes R,Schwenty-Lara J,Freese L,Neuhofer C,Möller J,Wehner P,van Ravenswaaij-Arts CMA,Wong MTY,Schanze I,Tzschach A,Bartsch O,Borchers A,Pauli S, Hum Mol Genet. April 15, 2018; 27(8):1460-2083. |