(Q33917461)

30 July 2017

Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2. (English)

1 reference

30 July 2017

8

Giddings JC

1 reference

30 July 2017

Tamagaki A

1

1 reference

30 July 2017

Shima M

2

1 reference

30 July 2017

Tomita R

3

1 reference

30 July 2017

Okumura M

4

1 reference

30 July 2017

Shibata M

5

1 reference

30 July 2017

Morichika S

6

1 reference

30 July 2017

Kurahashi H

7

1 reference

30 July 2017

Yoshioka A

9

1 reference

30 July 2017

Yokobayashi Y

10

1 reference

30 July 2017

language of work or name

1 reference

1 September 2000

1 reference

American Journal of Medical Genetics Part A

30 July 2017

1 reference

30 July 2017

94

1 reference

30 July 2017

1

1 reference

30 July 2017

5-8

1 reference

An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes

30 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Molecular genetics of familial spastic paraplegia: a multitude of responsible genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Isolation and characterization of a novel gene deleted in DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

The mobile nature of acrocentric elements illustrated by three unusual chromosome variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Evidence of a third locus in X-linked recessive spastic paraplegia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000904%2994%3A1%3C5%3A%3AAID-AJMG2%3E3.0.CO%3B2-O

10.1002/1096-8628(20000904)94:1<5::AID-AJMG2>3.0.CO;2-O

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference