(Q24616239)

15

object named as

Christine Klein

0 references

Laurie Ozelius

13

object named as

Laurie Ozelius

0 references

Vladimir S. Kostić

14

object named as

Vladimir Kostic

0 references

author name string

Birgitt Müller

1

0 references

Katja Hedrich

2

0 references

Norman Kock

3

0 references

Natasa Dragasevic

4

0 references

Marina Svetel

5

0 references

Jennifer Garrels

6

0 references

Olfert Landt

7

0 references

Matthias Nitschke

8

0 references

Peter P Pramstaller

9

0 references

Eberhard Schwinger

11

0 references

Jürgen Sperner

American Journal of Human Genetics

12

0 references

language of work or name

English

0 references

publication date

December 2002

0 references

published in

0 references

volume

71

0 references

issue

6

0 references

page(s)

1303-11

0 references

cites work

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Imprinting-mutation mechanisms in Prader-Willi syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

DNA methylation and genomic imprinting

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Genomic imprinting. Silence across the border.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378568

Inherited myoclonus-dystonia syndrome

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12444570

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/344531

1 reference

1 reference

1 reference

PubMed publication ID

12444570

1 reference