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Items: 1 to 20 of 65

1.

[Prevention of deafness based on genetic screening and testing].

Dai P, Yuan YY.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):973-7. Chinese. No abstract available.

PMID:
24506994
2.

The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect.

Bradley WG, Richardson J, Frew IJ.

Brain. 1974 Sep;97(3):521-32. No abstract available.

PMID:
4213898
3.

[Prevention and interdiction on hereditary deafness].

Dai P.

Zhonghua Yi Xue Za Zhi. 2007 Oct 30;87(40):2811-3. Chinese. No abstract available.

PMID:
18167281
4.

[Genetic screening for deafness].

Herberhold C.

HNO. 1999 May;47(5):456. German. No abstract available.

PMID:
10412653
5.

Genetic testing for deafness is here, but how do we do it?

Robin NH.

Genet Med. 2004 Nov-Dec;6(6):463-4. No abstract available.

PMID:
15545740
6.

The implications of genetic testing for deafness.

Arnos KS.

Ear Hear. 2003 Aug;24(4):324-31. Review.

PMID:
12923423
7.

Congenital heart disease, deafness, and skeletal malformations: a new syndrome?

Forney WR, Robinson SJ, Pascoe DJ.

J Pediatr. 1966 Jan;68(1):14-26. No abstract available.

PMID:
5901343
8.

[Diagnosis and prevention of genetic deafness: progress and attention].

Yang T.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Nov;28(22):1736-40. Chinese. No abstract available.

PMID:
25752101
9.

Psychological implications of genetic screening.

Marteau TM.

Birth Defects Orig Artic Ser. 1992;28(1):185-90.

PMID:
1340229
10.

Parental attitudes toward genetic testing for prelingual deafness in China.

Fu S, Dong J, Wang C, Chen G.

Int J Pediatr Otorhinolaryngol. 2010 Oct;74(10):1122-5. doi: 10.1016/j.ijporl.2010.06.012. Epub 2010 Jul 15.

PMID:
20637511
11.

Early identification of hearing-impaired infants.

Donahue A, Allen MP.

Neonatal Netw. 1999 Apr;18(3):58. No abstract available.

PMID:
10418439
12.

Attitudes of deaf individuals towards genetic testing.

Taneja PR, Pandya A, Foley DL, Nicely LV, Arnos KS.

Am J Med Genet A. 2004 Sep 15;130A(1):17-21.

PMID:
15368489
13.

["Genetization" of prenatal medicine].

Schmidtke J.

Z Geburtshilfe Neonatol. 1998 Jan-Feb;202(1):1. German. No abstract available.

PMID:
9577914
14.

Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures?

Nahar R, Puri RD, Saxena R, Verma IC.

Am J Med Genet A. 2013 Jan;161A(1):76-81. doi: 10.1002/ajmg.a.35692. Epub 2012 Dec 3.

PMID:
23208825
15.

In one's own image: ethics and the reproduction of deafness.

Johnston T.

J Deaf Stud Deaf Educ. 2005 Fall;10(4):426-41. Epub 2005 Jul 6.

PMID:
16000688
16.

[Prenatal screening for abnormalities and chromosomal disorders].

Brandt NJ, Skovby F.

Ugeskr Laeger. 1996 Feb 26;158(9):1197. Danish. No abstract available.

PMID:
8644422
17.

[Genetic consequences of cosanguinity].

Maximilian C, Toncescu N, Pop TV, Duca-Marinescu D.

Rev Pediatr Obstet Ginecol Pediatr. 1976 Oct-Dec;25(4):373-8. Romanian. No abstract available.

PMID:
139666
18.

Laboratory screening for genetic disorders and birth defects.

Bamforth FJ.

Clin Biochem. 1994 Oct;27(5):333-42. Review.

PMID:
7867213
19.

Non-invasive prenatal diagnosis: improved detection rates.

Panigrahi I, Thakur S, Murthy S.

Prenat Diagn. 2011 Feb;31(2):221. doi: 10.1002/pd.2658. No abstract available.

PMID:
21268045
20.

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.

Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.

Biochem Biophys Res Commun. 2006 Feb 3;340(1):194-9.

PMID:
16375862

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