Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome
about
Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosisIdentification of a novel single nucleotide polymorphism of HADHA gene at a referred primer-binding site during pre-diagnostic tests for preimplantation genetic diagnosis.
P2860
Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome
description
article
@en
im August 2001 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2001
@uk
ലേഖനം
@ml
name
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@en
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@nl
type
label
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@en
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@nl
prefLabel
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@en
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@nl
P2093
P356
P1476
Novel SNP at the common primer ...... s of craniosynostosis syndrome
@en
P2093
P304
P356
10.1002/AJMG.1461
P407
P50
P577
2001-08-01T00:00:00Z