These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
230 related articles for article (PubMed ID: 23918631)
1. Co-occurrence of 22q11 deletion syndrome and HDR syndrome. Fukai R; Ochi N; Murakami A; Nakashima M; Tsurusaki Y; Saitsu H; Matsumoto N; Miyake N Am J Med Genet A; 2013 Oct; 161A(10):2576-81. PubMed ID: 23918631 [TBL] [Abstract][Full Text] [Related]
2. A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess. Ikeuchi M; Kiyota K; Itonaga T; Kawano-Matsuda F; Ohata Y; Fujiwara M; Kubota T; Ozono K; Ihara K CEN Case Rep; 2021 May; 10(2):241-243. PubMed ID: 33159669 [TBL] [Abstract][Full Text] [Related]
3. HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report. Yang A; Kim J; Ki CS; Hong SH; Cho SY; Jin DK BMC Med Genet; 2017 Oct; 18(1):121. PubMed ID: 29073906 [TBL] [Abstract][Full Text] [Related]
4. Neonatal diagnosis of a patient with hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome associated with cerebral infarction. Mejia JD; Cervantes L; Puerta H; Bauer M; Diaz A J Pediatr Endocrinol Metab; 2014 Sep; 27(9-10):961-5. PubMed ID: 24859509 [TBL] [Abstract][Full Text] [Related]
5. Familial congenital choanal atresia with GATA3 associated hypoparathyroidism-deafness-renal dysplasia syndrome unidentified on auditory brainstem response. Kita M; Kuwata Y; Usui T Auris Nasus Larynx; 2019 Oct; 46(5):808-812. PubMed ID: 30396722 [TBL] [Abstract][Full Text] [Related]
6. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome. Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806 [TBL] [Abstract][Full Text] [Related]
7. A patient with 22q11.2 deletion syndrome: case report. Eryılmaz SK; Baş F; Satan A; Darendeliler F; Bundak R; Günöz H; Saka N J Clin Res Pediatr Endocrinol; 2009; 1(3):151-4. PubMed ID: 21274400 [TBL] [Abstract][Full Text] [Related]
11. A Unique Genomic Variant of HDR Syndrome in Newborn. Vidavalur R; Devapatla S Indian Pediatr; 2018 Aug; 55(8):705-706. PubMed ID: 30218523 [TBL] [Abstract][Full Text] [Related]
12. Clinical description of a patient carrying the smallest reported deletion involving 10p14 region. Melis D; Genesio R; Boemio P; Del Giudice E; Cappuccio G; Mormile A; Ronga V; Conti A; Imperati F; Nitsch L; Andria G Am J Med Genet A; 2012 Apr; 158A(4):832-5. PubMed ID: 22407589 [TBL] [Abstract][Full Text] [Related]
13. Associated anomalies in asymmetric crying facies and 22q11 deletion. Akcakus M; Ozkul Y; Gunes T; Kurtoglu S; Cetin N; Kisaarslan AP; Dundar M Genet Couns; 2003; 14(3):325-30. PubMed ID: 14577677 [TBL] [Abstract][Full Text] [Related]
14. Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion. Akçakuş M; Güneş T; Kurtoğlu S; Cetin N; Ozkul Y; Narin N; Atabek ME; Uğraş R Turk J Pediatr; 2004; 46(2):191-3. PubMed ID: 15214756 [TBL] [Abstract][Full Text] [Related]
15. Renal phenotypic variability in HDR syndrome: glomerular nephropathy as a novel finding. Chenouard A; Isidor B; Allain-Launay E; Moreau A; Le Bideau M; Roussey G Eur J Pediatr; 2013 Jan; 172(1):107-10. PubMed ID: 23052618 [TBL] [Abstract][Full Text] [Related]
16. Atypical copy number abnormalities in 22q11.2 region: report of three cases. Molck MC; Vieira TP; Sgardioli IC; Simioni M; Dos Santos AP; Souza J; Monteiro FP; Gil-da-Silva-Lopes VL Eur J Med Genet; 2013 Sep; 56(9):515-20. PubMed ID: 23886712 [TBL] [Abstract][Full Text] [Related]
17. De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome. Vittas S; Efstathiou G; Tsakalidis C; Malamaki C; Antari V; Chatzitoliou E; Chatziioannidis I; Galli-Tsinopoulou A; Soubasi V Cytogenet Genome Res; 2019; 158(1):32-37. PubMed ID: 30799418 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279 [TBL] [Abstract][Full Text] [Related]
19. Unusual Proliferative Glomerulonephritis in a Patient Diagnosed to Have Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome with a Novel Mutation in the GATA3 Gene. Kamezaki M; Kusaba T; Adachi T; Yamashita N; Nakata M; Ota N; Shiotsu Y; Ishida M; Usui T; Tamagaki K Intern Med; 2017; 56(11):1393-1397. PubMed ID: 28566604 [TBL] [Abstract][Full Text] [Related]
20. Clinical and molecular characteristics of two Italian kindreds with hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome. Dinoi E; Pierotti L; Mazoni L; Citro F; Della Valentina S; Sardella C; Borsari S; Michelucci A; Caligo MA; Marcocci C; Cetani F J Endocrinol Invest; 2024 Feb; 47(2):469-478. PubMed ID: 37561279 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]