BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 25771973)

  • 1. Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing.
    Lin YH; Wu CC; Hsu TY; Chiu WY; Hsu CJ; Chen PL
    Mutat Res; 2015 Jan; 771():1-5. PubMed ID: 25771973
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical Auditory Phenotypes Associated with
    Wang L; Lin QF; Wang HY; Guan J; Lan L; Xie LY; Yu L; Yang J; Zhao C; Liang JL; Zhou HL; Yang HM; Xiong WP; Zhang QJ; Wang DY; Wang QJ
    Chin Med J (Engl); 2017 Mar; 130(6):703-709. PubMed ID: 28303854
    [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. 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]  

  • 5. The first Korean case of HDR syndrome confirmed by clinical and molecular investigation.
    Cheon CK; Kim GH; Yoo HW
    Yonsei Med J; 2015 Jan; 56(1):300-3. PubMed ID: 25510779
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Audiometric characteristics of a dutch family with a new mutation in GATA3 causing HDR syndrome.
    van Beelen E; Leijendeckers JM; Admiraal RJ; Huygen PL; Hoefsloot LH; Pennings RJ; Snik AF; Kunst HP
    Audiol Neurootol; 2014; 19(2):106-14. PubMed ID: 24434941
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel GATA3 nonsense mutation in a newly diagnosed adult patient of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.
    Nanba K; Usui T; Nakamura M; Toyota Y; Hirota K; Tamanaha T; Kawashima ST; Nakao K; Yuno A; Tagami T; Naruse M; Shimatsu A
    Endocr Pract; 2013; 19(1):e17-20. PubMed ID: 23186964
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel de novo GATA3 mutation in a patient with HDR syndrome.
    Chen L; Chen B; Leng W; Lui X; Wu Q; Ouyang X; Liang Z
    J Int Med Res; 2015 Oct; 43(5):718-24. PubMed ID: 26268891
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification of a novel insertion mutation in GATA3 with HDR syndrome.
    Mino Y; Kuwahara T; Mannami T; Shioji K; Ono K; Iwai N
    Clin Exp Nephrol; 2005 Mar; 9(1):58-61. PubMed ID: 15830275
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome.
    Yeşiltepe Mutlu G; Kırmızıbekmez H; Nakamura A; Fukami M; Hatun Ş
    J Clin Res Pediatr Endocrinol; 2015 Dec; 7(4):344-8. PubMed ID: 26777049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Case of HDR Syndrome and Ichthyosis: Dual Diagnosis by Whole-Genome Sequencing of Novel Mutations in GATA3 and STS Genes.
    Goodwin G; Hawley PP; Miller DT
    J Clin Endocrinol Metab; 2016 Mar; 101(3):837-40. PubMed ID: 26731259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The syndrome of hypoparathyroidism, deafness, and renal anomalies.
    Upadhyay J; Steenkamp DW; Milunsky JM
    Endocr Pract; 2013; 19(6):1035-42. PubMed ID: 23757620
    [TBL] [Abstract][Full Text] [Related]  

  • 15. GATA3 abnormalities in six patients with HDR syndrome.
    Fukami M; Muroya K; Miyake T; Iso M; Kato F; Yokoi H; Suzuki Y; Tsubouchi K; Nakagomi Y; Kikuchi N; Horikawa R; Ogata T
    Endocr J; 2011; 58(2):117-21. PubMed ID: 21242646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome.
    Nakamura A; Fujiwara F; Hasegawa Y; Ishizu K; Mabe A; Nakagawa H; Nagasaki K; Jo W; Tajima T
    Endocr J; 2011; 58(2):123-30. PubMed ID: 21157112
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Novel
    Chu XY; Li YP; Nie M; Wang O; Jiang Y; Li M; Xia WB; Xing XP
    Chin Med J (Engl); 2017 Jun; 130(11):1378-1380. PubMed ID: 28524840
    [No Abstract]   [Full Text] [Related]  

  • 18. The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome.
    Döneray H; Usui T; Kaya A; Dönmez AS
    J Clin Res Pediatr Endocrinol; 2015 Jun; 7(2):140-3. PubMed ID: 26316437
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel loss-of-function mutation of GATA3 (p.R299Q) in a Japanese family with Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) syndrome.
    Okawa T; Yoshida M; Usui T; Kudou T; Iwasaki Y; Fukuoka K; Takahashi N; Uehara Y; Oiso Y
    BMC Endocr Disord; 2015 Oct; 15():66. PubMed ID: 26514990
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).
    Adachi M; Tachibana K; Asakura Y; Tsuchiya T
    J Pediatr Endocrinol Metab; 2006 Jan; 19(1):87-92. PubMed ID: 16509533
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.