Clinical presentation of a variant of Axenfeld-Rieger syndrome associated with subtelomeric 6p deletion.
about
Axenfeld-Rieger anomaly and Axenfeld-Rieger syndrome: clinical, molecular-cytogenetic, and DNA array analyses of three patients with chromosomal defects at 6p25Primary cellular meningeal defects cause neocortical dysplasia and dyslamination.PITX2 and FOXC1 spectrum of mutations in ocular syndromesUnexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridizationPhenotype of a Belgian Family With 6p25 Deletion Syndrome.Clinical expression of an inherited unbalanced translocation in chromosome 6.Pre- and postnatal phenotype of 6p25 deletions involving theFOXC1gene
P2860
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P2860
Clinical presentation of a variant of Axenfeld-Rieger syndrome associated with subtelomeric 6p deletion.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年學術文章
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name
Clinical presentation of a var ...... with subtelomeric 6p deletion.
@en
Clinical presentation of a var ...... with subtelomeric 6p deletion.
@nl
type
label
Clinical presentation of a var ...... with subtelomeric 6p deletion.
@en
Clinical presentation of a var ...... with subtelomeric 6p deletion.
@nl
prefLabel
Clinical presentation of a var ...... with subtelomeric 6p deletion.
@en
Clinical presentation of a var ...... with subtelomeric 6p deletion.
@nl
P2093
P50
P1476
Clinical presentation of a var ...... with subtelomeric 6p deletion
@en
P2093
Carmen Ramos
Dan Diego-Alvarez
Darryl Y Nishimura
Isabel Lorda-Sanchez
Marta Rodriguez de Alba
Pedro Ruiz-Barnes
P304
P356
10.1016/J.EJMG.2006.10.005
P577
2006-10-28T00:00:00Z