All individuals with variants in gene NR2F2

7 entries on 1 page. Showing entries 1 - 7.
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00132767 Patients Patients - - no China - - - - - CHTD congenital heart defect; double outlet right ventricle and ventricular septal defect 1 1 Yi-Qing Yang
00155734 29478779-Pat1 PubMed: Bashamboo 2018 2-generation family, 1 affected, unaffected non-carrier parents M no - Latino - - - - ? see paper; hypoplastic L heart at birth; severely dilated R ventricle with moderate RVH and mild to moderately depressed RV systolic function; male, hyperpigmented; phallus 3 cm with no hypospadias; gonads not palpable; ultra-sound no uterus, no gonads; left congenital diaphragmatic hernia 1 1 Johan den Dunnen
00155735 29478779-Pat2 PubMed: Bashamboo 2018 - M no Senegal - - - - - ? persistent ostium secundum, atrial septal defect, 1 1 Johan den Dunnen
00155736 29478779-Pat3 PubMed: Bashamboo 2018 - M no Hungary - - - - - ? 1d-ventricular septal defect; 9y-spontaneous closure ventricular septal defect; "ambiguous" Prader IV, pigmented scrotum, phallus-like clitoris, R palpable gonad in the inguinal canal; R ductus-like Wolffian structures, L uterus, ovary, and Fallopian tube, vagina and short urogenital sinus; pelvic ultrasound: R testis, L ovary, histology: R gonad, testis tubules, and ovarian tissue with oocytes; mild learning disabilities, minor limb anomalies, hypertelorism, blepharophimosis ptosis epicanthus inversus syndrome 1 1 Johan den Dunnen
00316125 K180 PubMed: Heidet 2017 affected patient and 1st degree relative - - France - - - - - CAKUT renal hypoplasia 1 2 Johan den Dunnen
00443816 Pat620 PubMed: Imafidon 2021 - F - Netherlands - - - - - ? cardiac malformation, dysmorphic features 1 1 Johan den Dunnen
00469167 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
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