Recurrence of urorectal septum malformation sequence spectrum anomalies in siblings: Time to explore the genetics
Author:
Affiliation:
1. Department of Medical Genetics; Nizam's Institute of Medical Sciences; Hyderabad; India
2. Department of Medical Genetics; Sanjay Gandhi Postgraduate Institute of Medical Sciences; Lucknow; India
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35950/fullpdf
Reference27 articles.
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2. Involvement of the HLXB9 homeobox gene in Currarino syndrome;Belloni;Am J Hum Genet,2000
3. Is urorectal septum malformation sequence a variant of the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association? Report of a case and a review of the literature;Chien;Eur J Pediatr,2005
4. Hoxd-13 expression in the development of hindgut in ethylenethiourea-exposed fetal rats;Dan;J Pediatr Surg,2010
5. Bidirectional signaling mediated by ephrin-B2 and EphB2 controls urorectal development;Dravis;Dev Biol,2004
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1. A fetus of partial urorectal septum malformation sequence characterized by complete septate uterus: A case report;Medicine;2023-03-31
2. Clinically diverse and perinatally lethal syndromes with urorectal septum malformation sequence;American Journal of Medical Genetics Part A;2022-12-07
3. Complete urorectal septal malformation with left hemimelia in a neonate: an uncommon association;BMJ Case Reports;2021-03
4. Clinical and risk factor analysis of cloacal defects in the National Birth Defects Prevention Study;American Journal of Medical Genetics Part A;2017-09-28
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