(Q41921167)

14 October 2017

A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome (English)

1 reference

14 October 2017

8

Norio Niikawa

1 reference

14 October 2017

Naoki Harada

1

1 reference

14 October 2017

Remco Visser

2

1 reference

14 October 2017

Angie Dawson

3

1 reference

14 October 2017

Makoto Fukamachi

4

1 reference

14 October 2017

Mie Iwakoshi

5

1 reference

14 October 2017

Nobuhiko Okamoto

6

1 reference

14 October 2017

Tatsuya Kishino

7

1 reference

14 October 2017

Naomichi Matsumoto

9

1 reference

14 October 2017

16 July 2004

1 reference

Journal of Human Genetics

14 October 2017

1 reference

14 October 2017

49

1 reference

14 October 2017

440-444

1 reference

14 October 2017

8

1 reference

https://scigraph.springernature.com/pub.10.1007/s10038-004-0166-z

14 October 2017

0 references

cites work

E2F-6, a member of the E2F family that can behave as a transcriptional repressor

1 reference

12 December 2020

Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation

1 reference

12 December 2020

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

1 reference

12 December 2020

Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity

1 reference

12 December 2020

9q34.3 deletion syndrome in three unrelated children.

1 reference

12 December 2020

Improved telomere detection using a telomere repeat probe (TTAGGG)n generated by PCR.

1 reference

12 December 2020

A PKC epsilon-ENH-channel complex specifically modulates N-type Ca2+ channels

1 reference

12 December 2020

Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.

1 reference

12 December 2020

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1 reference

12 December 2020

MIZIP, a highly conserved, vertebrate specific melanin-concentrating hormone receptor 1 interacting zinc-finger protein

1 reference

12 December 2020

Structure and functional expression of an omega-conotoxin-sensitive human N-type calcium channel

1 reference

12 December 2020

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

1 reference

12 December 2020

Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone-releasing hormone (LHRH) neurons

1 reference

12 December 2020

An optimized set of human telomere clones for studying telomere integrity and architecture.

1 reference

12 December 2020

Telomeres: a diagnosis at the end of the chromosomes

1 reference

12 December 2020

10.1007/S10038-004-0166-Z

Identifiers

DOI

1 reference

14 October 2017

1 reference