Congenital hypotonia in a child with a de novo 22q13 monosomy and 2pter duplication: a clinical and molecular genetic study. (Q51898506)
Jump to navigation
Jump to search
scientific article published on 4 October 2010
Language | Label | Description | Also known as |
---|---|---|---|
English | Congenital hypotonia in a child with a de novo 22q13 monosomy and 2pter duplication: a clinical and molecular genetic study. |
scientific article published on 4 October 2010 |
Statements
1 reference
Congenital hypotonia in a child with a de novo 22q13 monosomy and 2pter duplication: a clinical and molecular genetic study. (English)
1 reference
Antonio Trabacca
1 reference
Luciana Losito
1 reference
Marta De Rinaldis
1 reference
Leonarda Gennaro
1 reference
4 October 2010
1 reference
26
1 reference
2
1 reference
235-238
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference