Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
about
Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian familiesCase report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB.Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions.Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.
P2860
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
description
1997 nî lūn-bûn
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1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
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name
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
@en
type
label
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
@en
prefLabel
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
@en
P2093
P356
P1476
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
@en
P2093
C E de Die-Smulders
J J Engelen
J J Schrander
K E Chandler
P2888
P304
P356
10.1007/S004310050681
P577
1997-08-01T00:00:00Z