Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.
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Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderMouse Models of 22q11.2-Associated Autism Spectrum DisorderHomozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmentA modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.Behavioral abnormalities are common and severe in patients with distal 22q11.2 microdeletions and microduplications.Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb DuplicationHigh-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.Distal 22q11.2 Microduplication: Case Report and Review of the Literature.
P2860
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P2860
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.
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2010 nî lūn-bûn
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name
Sixteen New Cases Contributing ...... tal 22q11.2 Microduplications.
@en
Sixteen New Cases Contributing ...... tal 22q11.2 Microduplications.
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type
label
Sixteen New Cases Contributing ...... tal 22q11.2 Microduplications.
@en
Sixteen New Cases Contributing ...... tal 22q11.2 Microduplications.
@nl
prefLabel
Sixteen New Cases Contributing ...... tal 22q11.2 Microduplications.
@en
Sixteen New Cases Contributing ...... tal 22q11.2 Microduplications.
@nl
P2093
P2860
P50
P356
P1476
Sixteen New Cases Contributing ...... stal 22q11.2 Microduplications
@en
P2093
B B de Vries
B W M van Bon
B-M Anderlid
C Marcelis
D D A Keays
E M H F Bongers
H R Slater
P2860
P304
P356
10.1159/000327982
P577
2010-01-01T00:00:00Z