Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
about
The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2Localization of the human UbB polyubiquitin gene to chromosome band 17p11.1-17p12Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions.Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients
P2860
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
description
1988 nî lūn-bûn
@nan
1988 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
@ast
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
@en
type
label
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
@ast
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
@en
prefLabel
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
@ast
Chromosome subband 17p11.2 deletion: a minute deletion syndrome.
@en
P2093
P2860
P356
P1476
Chromosome subband 17p11.2 deletion: a minute deletion syndrome
@en
P2093
D Lockwood
J Allanson
T H Rizkallah
T M Goodwin
P2860
P304
P356
10.1136/JMG.25.11.732
P407
P577
1988-11-01T00:00:00Z