Within recent years, numerous individuals have been identified with terminal 4p microdeletions distal to the currently described critical regions for the Wolf-Hirschhorn syndrome (WHS). Some of these individuals do not display features consistent with WHS whereas others have a clinical phenotype with some overlap to the WHS phenotype. In this review we discuss the genetic and clinical presentation of these cases in an attempt to understand the consequence of monosomy of the genes distal to the proposed critical regions and identify the distal boundary for pathogenic genes involved in components of the WHS phenotype.status: publishe
A total of five Wolf-Hirschhorn syndrome (WHS) patient with a 4p16.3 de novo microdeletion was refer...
Wolf-Hirschhorn Syndrome (WHS) is caused by deletions on chromosome 4p and is clinically well define...
Background Wolf-Hirschhorn syndrome (WHS) results from the partial deletion of 4p. This study aimed ...
Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...
Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...
In an attempt to define the distinctive Wolf-Hirschhorn syndrome (WHS) phenotype, and to map its spe...
We report on a clinical-genetic study of 16 Wolf-Hirschhorn syndrome (WHS) patients. Hemizygosity of...
Recently the genotype/phenotype map of Wolf-Hirschhorn syndrome (WHS) has been refined, using small ...
Copyright © 2012 F. Sheth et al. This is an open access article distributed under the Creative Commo...
Based on genotype-phenotype correlation analysis of 80 Wolf-Hirschhorn syndrome (WHS) patients, as w...
Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene...
Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene...
Wolf–Hirschhorn syndrome (WHS) is a multiple malformation syndrome characterised by mental and devel...
The aim of this study was to obtain a quantitative definition of Wolf-Hirschhorn syndrome (WHS) thro...
Background: The Wolf-Hirschhorn syndrome (WHS) is usually caused by terminal deletions of the short ...
A total of five Wolf-Hirschhorn syndrome (WHS) patient with a 4p16.3 de novo microdeletion was refer...
Wolf-Hirschhorn Syndrome (WHS) is caused by deletions on chromosome 4p and is clinically well define...
Background Wolf-Hirschhorn syndrome (WHS) results from the partial deletion of 4p. This study aimed ...
Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...
Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...
In an attempt to define the distinctive Wolf-Hirschhorn syndrome (WHS) phenotype, and to map its spe...
We report on a clinical-genetic study of 16 Wolf-Hirschhorn syndrome (WHS) patients. Hemizygosity of...
Recently the genotype/phenotype map of Wolf-Hirschhorn syndrome (WHS) has been refined, using small ...
Copyright © 2012 F. Sheth et al. This is an open access article distributed under the Creative Commo...
Based on genotype-phenotype correlation analysis of 80 Wolf-Hirschhorn syndrome (WHS) patients, as w...
Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene...
Deletions in the 4p16.3 region are associated with Wolf-Hirschhorn syndrome (WHS), a contiguous gene...
Wolf–Hirschhorn syndrome (WHS) is a multiple malformation syndrome characterised by mental and devel...
The aim of this study was to obtain a quantitative definition of Wolf-Hirschhorn syndrome (WHS) thro...
Background: The Wolf-Hirschhorn syndrome (WHS) is usually caused by terminal deletions of the short ...
A total of five Wolf-Hirschhorn syndrome (WHS) patient with a 4p16.3 de novo microdeletion was refer...
Wolf-Hirschhorn Syndrome (WHS) is caused by deletions on chromosome 4p and is clinically well define...
Background Wolf-Hirschhorn syndrome (WHS) results from the partial deletion of 4p. This study aimed ...