A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
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Use of Targeted Exome Sequencing for Molecular Diagnosis of Skeletal DisordersPITX2 and FOXC1 spectrum of mutations in ocular syndromesPhenotype of a Belgian Family With 6p25 Deletion Syndrome.Whole exome association of rare deletions in multiplex oral cleft families.Gross chromosomal rearrangement mediated by DNA replication in stressed cells: evidence from Escherichia coli.Pre- and postnatal phenotype of 6p25 deletions involving theFOXC1gene
P2860
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
description
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name
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@en
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@nl
type
label
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@en
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@nl
prefLabel
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@en
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@nl
P2093
P2860
P356
P1476
A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
@en
P2093
Jeffrey W Innis
Jirair K Bedoyan
Marci M Lesperance
Ramaswamy K Iyer
Todd Ackley
P2860
P304
P356
10.1002/AJMG.A.33751
P407
P577
2010-12-10T00:00:00Z