4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohortIntergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.DiGeorge-like syndrome in a child with a 3p12.3 deletion involving MIR4273 gene born to a mother with gestational diabetes mellitus.
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4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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scientific article published on 22 July 2011
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wetenschappelijk artikel
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наукова стаття, опублікована в липні 2011
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name
4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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type
label
4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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prefLabel
4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
@en
4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
@nl
P2093
P2860
P1476
4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome
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P2093
Aleksandar Krstic
Danijela Drakulic
Goran Cuturilo
Ida Jovanovic
Vojislav Parezanovic
P2860
P2888
P304
P356
10.1007/S00431-011-1533-3
P577
2011-07-22T00:00:00Z