Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome. (2015)

First Author: Ellingford JM
Attributed to:  Molecular bases of congenital bladder disease: the urofacial syndome (UFS) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/s0140-6736(15)60496-2

PubMed Identifier: 25987160

Publication URI: http://europepmc.org/abstract/MED/25987160

Type: Journal Article/Review

Volume: 385

Parent Publication: Lancet (London, England)

Issue: 9980

ISSN: 0140-6736