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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

592 related items for PubMed ID: 30368370

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  • 3. Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families.
    Yin A, Liu C, Zhang Y, Wu J, Mai M, Ding H, Yang J, Zhang X.
    Int J Pediatr Otorhinolaryngol; 2014 Aug; 78(8):1356-9. PubMed ID: 24913939
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  • 4. [Screening for hotspot mutations associated with genetic hearing impairment in pregnant women and subsequent prenatal diagnosis in high risk pregnancies].
    Yang K, Qi H, Huang SS, Wen XH, Zhu JJ, Cai LR, Zeng W, Tang GD, Luo Y, Kang DY.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Sep 07; 53(9):645-649. PubMed ID: 30293254
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  • 5. [Prenatal diagnosis for hereditary deaf families assisted by genetic testing].
    Han B, Dai P, Qi QW, Wang LX, Wang Y, Bian XM, Wang QJ, Zhang X, Kang DY, Wang GJ, Han DY.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Sep 07; 42(9):660-3. PubMed ID: 18051563
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  • 7. [Analysis and prenatal diagnosis of deafness-related gene mutations in patients with nonsyndromic hearing loss].
    Li H, Chen Y, Mao Y, Ding Y, Xu X, Tang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct 07; 31(5):553-6. PubMed ID: 25297579
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  • 8. [Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].
    Dai P, Han B, Yuan YY, Jin ZC, Wang Y, Xiang Y, Yu F, Liu X, Wang GJ, Kang DY, Zhang X, Li M, Zhai SQ, Huang DL, Han DY.
    Zhonghua Yi Xue Za Zhi; 2007 Apr 24; 87(16):1088-92. PubMed ID: 17672986
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  • 9. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
    Riahi Z, Chahed H, Jaafoura H, Zainine R, Messaoud O, Naili M, Nagara M, Hammami H, Laroussi N, Bouyacoub Y, Kefi R, Bonnet C, Besbes G, Abdelhak S.
    Int J Pediatr Otorhinolaryngol; 2013 Sep 24; 77(9):1485-8. PubMed ID: 23856379
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  • 13. [A follow-up study of abnormal mutation in neonatal deafness gene screening].
    Liu QM, Tian Y, Yu JJ, He QQ, Peng L, Guo XQ, Li DY, Chen T.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Dec 07; 54(12):881-887. PubMed ID: 31887812
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  • 14. Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing.
    Bai X, Nian S, Feng L, Ruan Q, Luo X, Wu M, Yan Z.
    Mol Genet Genomic Med; 2019 Aug 07; 7(8):e808. PubMed ID: 31250571
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  • 17. A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.
    Jiang H, Niu Y, Qu L, Huang X, Zhu X, Tang G.
    Biosci Trends; 2018 Aug 07; 12(5):470-475. PubMed ID: 30473554
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  • 18. [Prenatal genetic counseling and instruction for deaf families by genetic test].
    Han MY, Huang SS, Wang GJ, Yuan YY, Kang DY, Zhang X, Dai P.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Nov 07; 46(11):909-13. PubMed ID: 22335977
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  • 19.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Smith RJH, Azaiez H, Booth K.
    ; 1993 Nov 07. PubMed ID: 20301449
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