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3. Early fetal presentation of Koolen-de Vries: Case report with literature review. Sauvestre F, Marguet F, Rooryck C, Vuillaume ML, Cardinaud F, Laquerrière A, André G, Pelluard F. Eur J Med Genet; 2017 Nov; 60(11):605-609. PubMed ID: 28811189 [Abstract] [Full Text] [Related]
4. [Koolen de Vries syndrome: A challenge in clinical practice]. Moreno Samos M, Moreno Medinilla EE, Martínez Antón JL, Urda Cardona A. An Pediatr (Barc); 2017 Mar; 86(3):162-164. PubMed ID: 27436569 [No Abstract] [Full Text] [Related]
8. 17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome. Bernardo P, Madia F, Santulli L, Del Gaudio L, Caccavale C, Zara F, Traverso M, Cirillo M, Striano S, Coppola A. Brain Dev; 2016 Aug; 38(7):663-8. PubMed ID: 26897099 [Abstract] [Full Text] [Related]
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17. Prenatal ultrasound findings in Koolen-de Vries foetuses: Central nervous system anomalies are frequent markers of this syndrome. García-Santiago FA, Martínez-Payo C, Mansilla E, Santos-Simarro F, Ruiz de Azua Ballesteros M, Mori MÁ, Antolín Alvarado E, Nieto Y, Vallcorba I, Tenorio J, Nevado J, Lapunzina P. Mol Genet Genomic Med; 2021 May 13; 9(5):e1649. PubMed ID: 33733630 [Abstract] [Full Text] [Related]