Prenatal Diagnosis for a Novel Splice Mutation of PHEX Gene in a Large Han Chinese Family Affected with X-Linked Hypophosphatemic Rickets-Reference-Cited by-同舟云学术

Prenatal Diagnosis for a Novel Splice Mutation of PHEX Gene in a Large Han Chinese Family Affected with X-Linked Hypophosphatemic Rickets

Author:

Qiu Guangrong¹,Liu Caixia²,Zhou Jingyi¹,Liu Peiyan¹,Wang Jun²,Jiang Hongkun¹³,Hou Zhiyan⁴,Zhao Yanyan¹,Sun Kailai¹,Li-Ling Jesse¹²⁵

Affiliation:

1. Department of Medical Genetics, School of Basic Medicine, China Medical University, Shenyang, China.

2. Liaoning Centre for Prenatal Diagnosis, Department of Gynecology and Obstetrics, Shengjing Hospital, China Medical University, Shenyang, China.

3. Department of Pediatrics, The First Affiliated Hospital, China Medical University, Shenyang, China.

4. Department of Obstetrics and Gynecology, Benxi Central Hospital, Benxi, China.

5. Sino-Dutch Biomedical and Information Engineering School, Northeastern University, Shenyang, China.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

Reference32 articles.

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