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1.
[Genetic and prenatal diagnosis for four families with Williams-Beuren syndrome].
Zhongguo Dang Dai Er Ke Za Zhi
; 17(12): 1267-72, 2015 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-26695662
2.
[Analysis of copy number variations in an infant with Cri du Chat syndrome by array-based comparative genomic hybridization].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(4): 443-6, 2013 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-23926013
3.
[Cytogenetic and molecular analysis of idic(Yp) in 1 infertile man and 1 prenatal fetus].
Zhonghua Nan Ke Xue
; 19(7): 642-6, 2013 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-23926684
4.
[A novel mutation Glu441stop (GAA to TAA) of androgen receptor gene resulting in complete androgen insensitivity syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 28(2): 176-9, 2011 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-21462130
5.
[Analysis of fetal chromosomal karyotype and etiology in 252 cases of early spontaneous abortion].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 28(5): 575-8, 2011 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-21983739
6.
[Karyotype analysis of chorionic villi from pregnant women with missed abortion using multiplex ligation-dependent probe amplification].
Zhonghua Fu Chan Ke Za Zhi
; 44(7): 509-13, 2009 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-19957550
7.
[One case of 2q37 deletion syndrome: clinical and genetic diagnosis].
Zhonghua Er Ke Za Zhi
; 51(12): 934-7, 2013 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-24495766
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