Tags

Type your tag names separated by a space and hit enter

A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome.
Clin Dysmorphol. 2016 Oct; 25(4):186-9.CD

Links

Publisher Full Text
Aggregator Full Text
Aggregator Full Text

Authors+Show Affiliations

Xiong S
aFetal Medicine Unit & Prenatal Diagnosis Centre Departments of bRadiology cGynecology, Shanghai First Maternity and Infant hospital, Tongji University School of Medicine, Shanghai, People's Republic of China dDepartment of Obstetrics and Gynecology, The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital eDepartment of Paediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada fDepartment of Medical Genomics, Royal Prince Alfred Hospital gDiscipline of Genetic Medicine and Centre for China Studies, University of Sydney, Sydney, New South Wales, Australia.
Chitayat D
No affiliation info available
Wei X
No affiliation info available
Zhu J
No affiliation info available
Lu W
No affiliation info available
Sun LM
No affiliation info available
Chopra M
No affiliation info available

MeSH

AllelesChild, PreschoolChinaCraniofacial AbnormalitiesDwarfismFaciesFemaleGenotypeHumansLimb Deformities, CongenitalMutationPhenotypeUrogenital AbnormalitiesWnt-5a Protein

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

27092434

Citation

Xiong, Shiyi, et al. "A Novel De-novo WNT5A Mutation in a Chinese Patient With Robinow Syndrome." Clinical Dysmorphology, vol. 25, no. 4, 2016, pp. 186-9.
Xiong S, Chitayat D, Wei X, et al. A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome. Clin Dysmorphol. 2016;25(4):186-9.
Xiong, S., Chitayat, D., Wei, X., Zhu, J., Lu, W., Sun, L. M., & Chopra, M. (2016). A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome. Clinical Dysmorphology, 25(4), 186-9. https://doi.org/10.1097/MCD.0000000000000130
Xiong S, et al. A Novel De-novo WNT5A Mutation in a Chinese Patient With Robinow Syndrome. Clin Dysmorphol. 2016;25(4):186-9. PubMed PMID: 27092434.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome. AU - Xiong,Shiyi, AU - Chitayat,David, AU - Wei,Xing, AU - Zhu,Jialiang, AU - Lu,Wen, AU - Sun,Lu Ming, AU - Chopra,Maya, PY - 2016/4/20/entrez PY - 2016/4/20/pubmed PY - 2017/2/7/medline SP - 186 EP - 9 JF - Clinical dysmorphology JO - Clin. Dysmorphol. VL - 25 IS - 4 SN - 1473-5717 UR - https://www.unboundmedicine.com/medline/citation/27092434/A_novel_de_novo_WNT5A_mutation_in_a_Chinese_patient_with_Robinow_syndrome_ L2 - http://dx.doi.org/10.1097/MCD.0000000000000130 DB - PRIME DP - Unbound Medicine ER -