scholarly journals Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism

2020 ◽  
Author(s):  
Chenyang Xu ◽  
Yanbao Xiang ◽  
Huanzheng Li ◽  
Yunzhi Xu ◽  
Yijian Mao ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Genetic Analysis ◽  
Oculocutaneous Albinism ◽  
Chinese Families

scholarly journals Genetic analysis and prenatal diagnosis of 76 Chinese families with X‐linked adrenoleukodystrophy

2021 ◽  
Author(s):  
Siwen Liu ◽  
Lin Li ◽  
Hairong Wu ◽  
Pei Pei ◽  
Xuefei Zheng ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Genetic Analysis ◽  
Chinese Families

Prenatal diagnosis of oculocutaneous albinism type II and novel mutations in two Chinese families

2007 ◽  
Vol 27 (6) ◽  
pp. 502-506 ◽  
Author(s):  
Li Hongyi ◽  
Wei Haiyun ◽  
Zheng Hui ◽  
Wenren Qing ◽  
Duan Honglei ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Oculocutaneous Albinism ◽  
Type Ii ◽  
Novel Mutations ◽  
Chinese Families

scholarly journals Prenatal Diagnosis of Oculocutaneous Albinism by Electron Microscopy of Fetal Skin

1983 ◽  
Vol 80 (3) ◽  
pp. 210-212 ◽  
Author(s):  
Robin A.J. Eady ◽  
David B. Gunner ◽  
Alec Garner ◽  
Charles H. Rodeck
Keyword(s):  
Electron Microscopy ◽  
Prenatal Diagnosis ◽  
Oculocutaneous Albinism ◽  
Fetal Skin

scholarly journals Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review

2016 ◽  
Vol 55 (5) ◽  
pp. 712-717 ◽  
Author(s):  
Chih-Ping Chen ◽  
Liang-Kai Wang ◽  
Schu-Rern Chern ◽  
Yen-Ni Chen ◽  
Shin-Wen Chen ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Literature Review ◽  
Genetic Analysis ◽  
Molecular Genetic ◽  
Molecular Genetic Analysis ◽  
Mosaic Trisomy

Clinical and genetic analysis for four Chinese families with Prader–Willi syndrome

Endocrine ◽  
2009 ◽  
Vol 36 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Yu-wen Zhang ◽  
Hui-ying Jia ◽  
Jie Hong ◽  
Yan Ge ◽  
Hui-jie Zhang ◽  
...  
Keyword(s):  
Genetic Analysis ◽  
Prader Willi Syndrome ◽  
Chinese Families

scholarly journals Mutational Analysis of TYR , OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism

2019 ◽  
Vol 7 (7) ◽  
Author(s):  
Ye Lin ◽  
Xihui Chen ◽  
Ying Yang ◽  
Fengyu Che ◽  
Sijia Zhang ◽  
...  
Keyword(s):  
Mutational Analysis ◽  
Oculocutaneous Albinism ◽  
Chinese Families
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