An interstitial deletion of chromosome 7 at band q21: a case report and review.
about
Prenatal diagnosis of a 7q21.13q22.1 deletion detected using high-resolution microarray.Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.7q21.11 Microdeletion in a Neonate With Goldenhar Syndrome: Case Report and a Literature Review.Functional characterization of tissue-specific enhancers in the DLX5/6 locus.Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay.Diagnostic yield of chromosomal microarray analysis in an autism primary care practice: which guidelines to implement?Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.Chromosomal rearrangements in patients with clinical features of Silver-Russell syndrome.
P2860
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P2860
An interstitial deletion of chromosome 7 at band q21: a case report and review.
description
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An interstitial deletion of chromosome 7 at band q21: a case report and review.
@en
An interstitial deletion of chromosome 7 at band q21: a case report and review.
@nl
type
label
An interstitial deletion of chromosome 7 at band q21: a case report and review.
@en
An interstitial deletion of chromosome 7 at band q21: a case report and review.
@nl
prefLabel
An interstitial deletion of chromosome 7 at band q21: a case report and review.
@en
An interstitial deletion of chromosome 7 at band q21: a case report and review.
@nl
P2093
P2860
P50
P356
P1476
An interstitial deletion of chromosome 7 at band q21: a case report and review.
@en
P2093
Jan Wauters
Katrien Storm
Lieve Nuytinck
Ludwine Messiaen
Nils Peeters
Stefan Vermeulen
Winnie Courtens
P2860
P356
10.1002/AJMG.A.30106
P407
P577
2005-04-01T00:00:00Z