(Q35196691)

7 August 2017

Genetic risks for children of women with myotonic dystrophy. (English)

1 reference

7 August 2017

Koch MC

1

1 reference

7 August 2017

Grimm T

series ordinal

2

1 reference

7 August 2017

Harley HG

series ordinal

3

1 reference

7 August 2017

Harper PS

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 June 1991

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

48

1 reference

7 August 2017

1084-1091

1 reference

7 August 2017

6

1 reference

Chromosomal imprinting and the parent transmission specific variation in expressivity of Huntington disease

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Clinical evidence for heterogeneity in myotonic dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Risk estimates for neonatal myotonic dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Neonatal myotonic dystrophy as a cause of hydramnios and neonatal death. A case report and literature review

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Early onset myotonic dystrophy. Clinical and laboratory findings in five families and a review of the literature

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Variants of myotonic dystrophy in pre-adolescent life (the syndrome of myotonic dysembryoplasia).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Genetic heterogeneity for dystrophia myotonica

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Hyperinsulinemia in myotonic dystrophy: identity of the maternal factor causing the neonatal myotonic dystrophy syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Neonatal Steinert's disease: apropos of 2 cases in 2 successive generations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Myotonic dystrophy and pregnancy: a review.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Genomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea

28 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

28 July 2018

12 December 2020

Congenital myotonic dystrophy: respiratory function at birth determines survival

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Neonatal respiratory failure due to myotonic dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Thin ribs in neonatal myotonic dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Congenital myotonic dystrophy in Britain. I. Clinical aspects

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Clinical effects of myotonic dystrophy on pregnancy and the neonate

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

MYOTONIC DYSTROPHY IN INFANCY AND CHILDHOOD

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Pregnancy in myotonica dystrophia; a case report.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Course, prognosis and complications of childhood-onset myotonic dystrophy

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Myotonic dystrophy: A neglectedcause of mental retardation

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Cystinuria with congenital myotonic dystrophy

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Immaturity of muscle fibers in the congenital form of myotonic dystrophy: its consequences and its origin.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683098

Mitochondrial DNA and genetic disease

26 September 2018

1 reference

12 December 2020

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus

1 reference

12 December 2020

The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus

1 reference

12 December 2020

Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting

1 reference

12 December 2020

Hydrops and pleural effusions in congenital myotonic dystrophy

1 reference

12 December 2020

Outlook for a clinically normal child in a sibship with congenital myotonic dystrophy

1 reference

12 December 2020

Myotonic dystrophy in the neonate

1 reference

12 December 2020

Congenital dystrophia myotonica

1 reference

12 December 2020

Myotonia dystrophica: obstetric complications

1 reference

12 December 2020

Survey of patients with early-onset myotonic dystrophy in the San-In district, Japan

1 reference

12 December 2020

Myotonic dystrophy: limited electromyographic abnormalities in 2 definite cases

1 reference

12 December 2020

Identifiers

PMCID

1683098

1 reference

7 August 2017

1 reference