Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

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http://www.wikidata.org/entity/Q34101094
The genetics of autistic disorders and its clinical relevance: a review of the literatureDelta/notch-like epidermal growth factor (EGF)-related receptor, a novel EGF-like repeat-containing protein targeted to dendrites of developing and adult central nervous system neuronsThe 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patientsHaploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.Social timing, clock genes and autism: a new hypothesis.Loss of heterozygosity at 2q37 in sporadic Wilms' tumor: putative role for miR-562.A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocationChromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.Mitochondrial and ion channel gene alterations in autism.Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4Presence of large deletions in kindreds with autism.Brief report: peculiar evolution of autistic behaviors in two unrelated children with brachidactyly-mental retardation syndrome.Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size.
P2860

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

Item
http://www.wikidata.org/entity/Q34101094
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Molecular genetic delineation ...... for deletion screening by PCR.
@ast
Molecular genetic delineation ...... for deletion screening by PCR.
@en
Molecular genetic delineation ...... for deletion screening by PCR.
@nl
type
label
Molecular genetic delineation ...... for deletion screening by PCR.
@ast
Molecular genetic delineation ...... for deletion screening by PCR.
@en
Molecular genetic delineation ...... for deletion screening by PCR.
@nl
prefLabel
Molecular genetic delineation ...... for deletion screening by PCR.
@ast
Molecular genetic delineation ...... for deletion screening by PCR.
@en
Molecular genetic delineation ...... for deletion screening by PCR.
@nl
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P698
P921
P356
P1433
P1476
Molecular genetic delineation ...... for deletion screening by PCR.
@en
P2093
P304
P31
P356
P433
P478
P577
P698
P921