Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree (Q37099823)
Jump to navigation
Jump to search
scientific article published on 16 July 2016
Language | Label | Description | Also known as |
---|---|---|---|
English | Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree |
scientific article published on 16 July 2016 |
Statements
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree (English)
Stylianos E Antonarakis
1 reference
1 reference