Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
about
Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.Mutation analysis of UBE3A in Angelman syndrome patients.Distinct phenotypes distinguish the molecular classes of Angelman syndromeJuxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotypeThe Largest Paracentric Inversion, the Highest Rate of Recombinant Spermatozoa. Case Report: 46,XY, inv(2)(q21.2q37.3) and Literature Review.
P2860
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
description
1997 nî lūn-bûn
@nan
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
@zh-cn
name
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@en
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@nl
type
label
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@en
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@nl
prefLabel
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@en
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@nl
P2093
P2860
P1476
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.
@en
P2093
J Wagstaff
S S Rosengren
P2860
P304
P407
P577
1997-03-01T00:00:00Z