Work

12 q deletion with oculodentodigital dysplasia -like phenotype

Year: 2016

Type: article

Source: Clinical Case Reports and Reviews

DOI: 10.15761/ccrr.1000224

Authors: Miguel Cano, Joseph Trapasso, Tabitha Trapasso, Reuben Matalon

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: hybrid

OpenAlex ID: W2421443978

FWCI: 0.269

Cites:

Cited by: 5

Related to: 10