Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report.
about
Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome: an update of the CREBBP deletion repertoire.Patent ductus arteriousus device closure in an infant with rubinstein-taybi syndrome.A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient.Sulfotransferase 1A3/4 copy number variation is associated with neurodegenerative disease.
P2860
Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report.
description
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name
Chromosomal 16p microdeletion ...... hybridization: a case report.
@ast
Chromosomal 16p microdeletion ...... hybridization: a case report.
@en
type
label
Chromosomal 16p microdeletion ...... hybridization: a case report.
@ast
Chromosomal 16p microdeletion ...... hybridization: a case report.
@en
prefLabel
Chromosomal 16p microdeletion ...... hybridization: a case report.
@ast
Chromosomal 16p microdeletion ...... hybridization: a case report.
@en
P2093
P2860
P356
P1476
Chromosomal 16p microdeletion ...... hybridization: a case report.
@en
P2093
Azli Ismail
Md A Mohd Fadley
Narazah Mohd Yusoff
Thong Meow Keong
Zubaidah Zakaria
P2860
P356
10.1186/1752-1947-6-30
P407
P577
2012-01-23T00:00:00Z