Emmanuelle Ranza
0000-0002-2131-5744
3 papers found
Refreshing results…
Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia
De novo variants in CELF2 that disrupt the nuclear localization signal cause developmental and epileptic encephalopathy
Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants
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