[Prenatal diagnosis for hereditary deaf families assisted by genetic testing].

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery

Volumn 42, Issue 9, 2007, Pages 660-663

  Han, Bing ^a   Dai, P ^b   Qi, Qing wei ^b   Wang, Long xia ^b   Wang, Y ^b   Bian, Xu ming ^b   Wang, Qiu ju ^b   Zhang, Xin ^b   Kang, Dong yang ^b   Wang, Guo jian ^b   Han, Dong yi ^b  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; CONNEXIN 26; GAP JUNCTION PROTEIN; MITOCHONDRIAL DNA; SLC26A4 PROTEIN, HUMAN;

ARTICLE; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; GENETICS; HEARING IMPAIRMENT; HOMOZYGOTE; HUMAN; MALE; NEWBORN; PREGNANCY; PRENATAL DIAGNOSIS;

CONNEXINS; DEAFNESS; DNA, MITOCHONDRIAL; FEMALE; GENETIC COUNSELING; GENETIC TESTING; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; MALE; MEMBRANE TRANSPORT PROTEINS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 80052592710     PISSN: 16730860     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)