1 |
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
|
|
|
|
BASE
|
|
Show details
|
|
2 |
Associations of HLA alleles with specific language impairment
|
|
|
|
BASE
|
|
Show details
|
|
3 |
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
|
|
|
|
BASE
|
|
Show details
|
|
4 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
|
|
|
|
BASE
|
|
Show details
|
|
5 |
Associations of HLA alleles with specific language impairment
|
|
|
|
BASE
|
|
Show details
|
|
6 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
|
|
|
|
BASE
|
|
Show details
|
|
7 |
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
|
|
|
|
BASE
|
|
Show details
|
|
8 |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
|
|
|
In: Human molecular genetics, vol 21, iss 21 (2012)
|
|
BASE
|
|
Show details
|
|
9 |
Individual common variants exert weak effects on the risk for autism spectrum disorders ...
|
|
|
|
BASE
|
|
Show details
|
|
10 |
Individual common variants exert weak effects on the risk for autism spectrum disorders
|
|
|
|
BASE
|
|
Show details
|
|
11 |
Individual common variants exert weak effects on risk for Autism Spectrum Disorders
|
|
|
|
BASE
|
|
Show details
|
|
12 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
|
|
|
|
BASE
|
|
Show details
|
|
13 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
|
|
|
|
BASE
|
|
Show details
|
|
14 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
|
|
|
|
BASE
|
|
Show details
|
|
15 |
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment
|
|
|
|
BASE
|
|
Show details
|
|
16 |
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
|
|
|
|
BASE
|
|
Show details
|
|
18 |
A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study
|
|
|
|
BASE
|
|
Show details
|
|
|
|