(Q24312410)

1

0 references

S M Walpole

2

0 references

A Nicolaou

3

0 references

P van der Bent

4

0 references

A Cahn

5

0 references

M Vaudin

6

0 references

M T Ross

7

0 references

J Durham

8

0 references

R Pavitt

9

0 references

J Wilkinson

10

0 references

D Grafham

11

0 references

A A Bergen

12

0 references

G J van Ommen

13

0 references

J R Yates

14

0 references

J T den Dunnen

15

0 references

D Trump

Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22

16

0 references

language of work or name

English

0 references

publication date

1 April 1998

0 references

published in

Genomics

0 references

volume

49

0 references

page(s)

96-102

0 references

issue

1

0 references

cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

High-resolution physical map of the X-linked retinoschisis interval in Xp22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Severe congenital limb deficiencies, vertebral hypersegmentation, absent thymus and mirror polydactyly: a defect expression of a developmental control gene?

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Fifteen dorsal vertebrae and rib pairs in two siblings

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

The Drosophila melanogaster tumor suppressor gene lethal(3)malignant brain tumor encodes a proline-rich protein with a novel zinc finger.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Locking in stable states of gene expression: transcriptional control during Drosophila development.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Transformation of axial skeleton due to overexpression of bmi-1 in transgenic mice

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Positional cloning of the gene associated with X-linked juvenile retinoschisis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Identification of Bmi1-interacting proteins as constituents of a multimeric mammalian polycomb complex

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

The polyhomeotic gene of Drosophila encodes a chromatin protein that shares polytene chromosome-binding sites with Polycomb

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Posterior transformation, neurological abnormalities, and severe hematopoietic defects in mice with a targeted deletion of the bmi-1 proto-oncogene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Identification and characterization of interactions between the vertebrate polycomb-group protein BMI1 and human homologs of polyhomeotic

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

X linked retinoschisis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Improved genetic mapping of X linked retinoschisis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021