Lara Hawkes1, Usha Kini. Show Affiliations » 1. Department of Clinical Genetics, Oxford University Hospitals NHS Trust, Oxford, UK.
Abstract
Entities: Disease
Mesh： See more » Child, PreschoolCryptorchidism/diagnosisCryptorchidism/geneticsCryptorchidism/physiopathologyFacial Paralysis/geneticsFacial Paralysis/physiopathologyFaciesFemaleGrowth Disorders/diagnosisGrowth Disorders/geneticsGrowth Disorders/physiopathologyHand Deformities, Congenital/diagnosisHand Deformities, Congenital/geneticsHand Deformities, Congenital/physiopathologyHumansHypertrophy/diagnosisHypertrophy/geneticsHypertrophy/physiopathologyInfant, NewbornIntellectual Disability/diagnosisIntellectual Disability/geneticsIntellectual Disability/physiopathologyJoint Diseases/diagnosisJoint Diseases/geneticsJoint Diseases/physiopathologyPulmonary Valve Stenosis/geneticsPulmonary Valve Stenosis/physiopathologySmad4 Protein/genetics
Substances： See more » SMAD4 protein, humanSmad4 Protein
Year: 2015 PMID： 25486016 DOI： 10.1097/MCD.0000000000000068
Source DB: PubMed Journal: Clin Dysmorphol ISSN： 0962-8827 Impact factor: 0.816