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1.
Genetic Analysis of a Case of Sotos Syndrome with Suspected Germinal Mosaicism in Mother.
Appl Biochem Biotechnol
; 195(10): 5792-5801, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-36708490
2.
Copy number variation analysis and outcomes of 1 658 fetuses with increased nuchal translucency / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
; (12): 26-32, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-995059
3.
Application of genomic copy number variation detection technology in prenatal diagnosis of 7617 pregnant women with serological screening abnormalities during the second trimester of pregnancy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 468-473, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-928439
4.
Early warning of low maternal unconjugated estriol level by prenatal screening for fetus with X-linked ichthyosis / 中华妇产科杂志
Chinese Journal of Obstetrics and Gynecology
; (12): 407-412, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-956670
5.
Risk analysis of recurrence of women with DMD birth history in families with new mutations in DMD gene / 中华检验医学杂志
Chinese Journal of Laboratory Medicine
; (12): 509-515, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-912435
6.
Experience in diagnosis and treatment of 10 COVID-19 patients with history of thoracotomy / 中华胸心血管外科杂志
Chinese Journal of Thoracic and Cardiovascular Surgery
; (12): 411-414, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-871638
7.
Genetic analysis of 90 families affected with spinal muscular atrophy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 116-122, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-781286
8.
Recurrent Angelman syndrome caused by a rare partial deletion of UBE3A gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 491-494, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-771982
9.
Analysis of ELN gene mutation in a pedigree affected with cutis laxa / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 785-788, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-776806
10.
Germinal mosaicism for partial deletion of the Dystrophin gene in a family affected with Duchenne muscular dystrophy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 1015-1018, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-776754
11.
Germinal mosaicism for partial deletion of the Dystrophin gene in a family affected with Duchenne muscular dystrophy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 1015-1018, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-796470
12.
Genetic analysis of a pedigree affected with distal hereditary motor neuronopathy V / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 207-211, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-775767
13.
Analysis of pathological mutation in a Chinese pedigree affected with familial exudative vitreoretinopathy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 193-196, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-687980
14.
Relationship between social support and mental health among nurses in China:a Meta- analysis / 中国实用护理杂志
Chinese Journal of Practical Nursing
; (36): 2548-2553, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-697393
15.
Genetic analysis for a haemophilia B family with multi nucleotides deletion mutation of F9 gene / 中华检验医学杂志
Chinese Journal of Laboratory Medicine
; (12): 675-679, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-712192
16.
Study on application of next-generation sequencing technology in diagnosis of cardio-facio-cutaneous syndrome / 重庆医学
Chongqing Medicine
; (36): 1074-1076, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-691916
17.
Combined Let-7a and H19 Signature: A Prognostic Index of Progression-Free Survival in Primary Breast Cancer Patients / 한국유방암학회지
Journal of Breast Cancer
; : 142-149, 2018.
Artículo
en Inglés
| WPRIM | ID: wpr-714867
18.
Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 266-269, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-335140
19.
Phenotypic diversity of human nature and induced CD4+CD25+FoxP3+CD127-regulatory T cells / 中国组织工程研究
Chinese Journal of Tissue Engineering Research
; (53): 236-241, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-487756
20.
Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 629-632, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-345394