Nan Bai - Publications

Mutation analysis and prenatal diagnosis for a pedigree affected with maple syrup urine disease

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: October 10, 2018

Mutations in the γ-secretase genes PSEN1, PSENEN, and NCSTN in a family with acne inversa.

Journal: European journal of dermatology : EJD

Published: August 15, 2018

Diagnosis of a case with recurrent pregnancy loss resulted from maternal balanced translocation by chromosomal microarray analysis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 14, 2018

Genetic and prenatal diagnosis of a retinitis pigmentosa pedigree

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 14, 2018

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: October 17, 2017

Factor VIII mutation spectrum in haemophilia A patients in the population of Henan, China.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: March 03, 2017

Genetic analysis for a family affected with hemophilia type A due to a large deletion of F8 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: December 17, 2016

Detection and genetic counseling of F8 gene inversions for patients with severe hemophilia A

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: July 26, 2016

Genetic analysis of a rare case with Kallman syndrome and steroid sulfatase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 07, 2016

SNP array and cytogenetic analysis of a patient with unexplained mental retardation

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 07, 2016

The predictive value of selected serum microRNAs for acute GVHD by TaqMan MicroRNA arrays.

Journal: Annals of hematology

Published: June 05, 2016

Genetic analysis of a patient featuring developmental delay and mental retardation

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 10, 2016