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1.
Noninvasive prenatal testing for the detection of fetal chromosome 17 microduplication: clinical implications and findings.
Mol Cytogenet
; 17(1): 10, 2024 Apr 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-38644482
2.
[Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 29(4): 404-7, 2012 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-22875495
3.
[Analysis of an hereditary protein C deficiency pedigree with compound heterozygous gene mutations].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 29(5): 515-8, 2012 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-23042384
4.
[Analysis of an hereditary coagulation factor XII deficiency in a consanguineous pedigree].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 28(6): 666-9, 2011 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-22161101
5.
Luteolin induces hippocampal neurogenesis in the Ts65Dn mouse model of Down syndrome.
Neural Regen Res
; 14(4): 613-620, 2019 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-30632501
6.
Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood.
J Int Med Res
; 45(2): 621-630, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28357876
7.
The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
Blood Coagul Fibrinolysis
; 25(8): 824-30, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-24911457
8.
[Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].
Zhonghua Xue Ye Xue Za Zhi
; 32(12): 854-7, 2011 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-22339961
9.
[Analysis of phenotype and genotype in a Chinese pedigree with inherited prothrombin deficiency resulted from a homozygous mutation Tyr510Asp].
Zhonghua Xue Ye Xue Za Zhi
; 33(7): 587-9, 2012 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-22967428
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