Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
about
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeThe neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.Spatial working memory in neurofibromatosis 1: Altered neural activity and functional connectivity.Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.Refined physical and genetic mapping of the NF1 region on chromosome 17Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints.A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type I.Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.Genetic analysis of eight loci tightly linked to neurofibromatosis 1Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.A search for evidence of somatic mutations in the NF1 gene.Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patientsDeletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients.The NF1 gene in tumor syndromes and melanoma.
P2860
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P2860
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@en
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@nl
type
label
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@en
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@nl
prefLabel
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@en
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@nl
P2093
P1433
P1476
Genetic analysis of NF1: identification of close flanking markers on chromosome 17.
@en
P2093
Goldgar DE
P304
P356
10.1016/0888-7543(87)90034-6
P577
1987-12-01T00:00:00Z