(Q22008834)

central nervous system development

GOA release 2020-03-11

1 reference

Three-generation pedigree of a Möbius syndrome variant with chromosome translocation

GOA release 2020-03-11

N Matsumoto

1

N

Matsumoto

1 reference

7 February 2023

D T Pilz

series ordinal

2

author given names

D T

author last names

Pilz

1 reference

7 February 2023

D H Ledbetter

series ordinal

3

author given names

D H

author last names

Ledbetter

1 reference

7 February 2023

language of work or name

English

0 references

publication date

1 March 1999

0 references

published in

Genomics

0 references

volume

56

0 references

issue

2

0 references

page(s)

179-83

0 references

cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Lissencephaly and other malformations of cortical development: 1995 update

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA clones encoding relatively large proteins

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021

Deletion of chromosome 13 in Moebius syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5673

7 January 2021