[1] |
Cheng Yanhui, Bao Ying, Qian Pei, Huang Huimei.
Clinical characteristics and genotype analysis of the child with Alport syndrome with GJB2 gene mutation-induced deafness: A case report and literature review
[J]. Clinical Focus, 2022, 37(4): 354-357.
|
[2] |
.
[J]. Clinical Focus, 2011, 26(22): 2011-2012.
|
[3] |
.
[J]. CLINICAL FOCUS, 2010, 25(21): 1918-1919.
|
[4] |
.
[J]. CLINICAL FOCUS, 2009, 24(18): 1602-1603.
|
[5] |
.
[J]. CLINICAL FOCUS, 2008, 23(3): 205-206.
|
[6] |
.
[J]. CLINICAL FOCUS, 2008, 23(3): 0-0.
|
[7] |
.
[J]. CLINICAL FOCUS, 2008, 23(1): 3-0.
|
[8] |
.
[J]. CLINICAL FOCUS, 2007, 22(6): 431-432.
|
[9] |
.
[J]. CLINICAL FOCUS, 2006, 21(17): 1281-1282.
|
[10] |
.
[J]. CLINICAL FOCUS, 2006, 21(13): 962-963.
|
[11] |
.
[J]. CLINICAL FOCUS, 2005, 20(2): 101-102.
|
[12] |
.
[J]. CLINICAL FOCUS, 2004, 19(24): 1393-1393.
|