Open AccessChromosome 1p31.1 deletion syndrome: Limited expression
Author(s) -
Sasmita Biswal,
Preetinanda Parida,
Aranya Dubbudu,
Indar Kumar Sharawat,
Prateek Kumar Panda
Publication year - 2021
Publication title -
annals of indian academy of neurology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 31
eISSN - 1998-3549
pISSN - 0972-2327
DOI - 10.4103/aian.aian_258_20
Subject(s) - microdeletion syndrome , intellectual disability , medicine , facial dysmorphism , pediatrics , bioinformatics , craniofacial , chromosome , genetics , gene , biology , psychiatry , phenotype