Open AccessBardet-Biedl Syndrome- Polydactyly with Multifarious Defects - A Rare Case Report
Author(s) -
P K Rejinraj,
S Chacko,
John Nobel Thomas,
K Sukanya,
Punnose Thomas Puthuveettil
Publication year - 2020
Publication title -
journal of evidence based medicine and healthcare
Language(s) - English
Resource type - Journals
eISSN - 2349-2570
pISSN - 2349-2562
DOI - 10.18410/jebmh/2020/127
Subject(s) - polydactyly , medicine , bardet–biedl syndrome , pediatrics , anatomy , genetics , biology , phenotype , gene