De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.
about
Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study.Paternally derived translocation t(8;18)(q22.1;q22)pat associated in a patient with developmental delay: Case report and reviewScreening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeresMolecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints.
P2860
De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.
description
1993 nî lūn-bûn
@nan
1993 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
De novo microdeletion on an in ...... alanced translocation carrier.
@ast
De novo microdeletion on an in ...... alanced translocation carrier.
@en
type
label
De novo microdeletion on an in ...... alanced translocation carrier.
@ast
De novo microdeletion on an in ...... alanced translocation carrier.
@en
prefLabel
De novo microdeletion on an in ...... alanced translocation carrier.
@ast
De novo microdeletion on an in ...... alanced translocation carrier.
@en
P2093
P2860
P1476
De novo microdeletion on an in ...... balanced translocation carrier
@en
P2093
P2860
P304
P407
P577
1993-09-01T00:00:00Z