Genetic risks for children of women with myotonic dystrophy.

THE EFFECT OF METHODS OF ASCERTAINMENT UPON THE ESTIMATION OF FREQUENCIES

1934 • 500 citations

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

1987 • 478 citations

Congenital myotonic dystrophy in Britain. I. Clinical aspects.

1975 • 170 citations

EARLY-ONSET DYSTROPHIA MYOTONICA EVIDENCE SUPPORTING A MATERNAL ENVIRONMENTAL FACTOR

1972 • 140 citations

MYOTONIC DYSTROPHY IN INFANCY AND CHILDHOOD

1965 • 104 citations

Clinical Effects of Myotonic Dystrophy on Pregnancy and the Neonate

1976 • 82 citations

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

1988 • 80 citations

Congenital dystrophia myotonica

1973 • 79 citations

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

1985 • 78 citations

Gentics 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

1983 • 69 citations

Congenital myotonic dystrophy: respiratory function at birth determines survival.

1989 • 69 citations

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

1988 • 67 citations

COURSE, PROGNOSIS AND COMPLICATIONS OF CHILDHOOD‐ONSET MYOTONIC DYSTROPHY

1984 • 63 citations

Myotonia dystrophica: Obstetric complications

1978 • 57 citations

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

1989 • 56 citations

Early Onset Myotonic Dystrophy

1967 • 52 citations

Myotonic dystrophy in the neonate

1972 • 52 citations

Myotonic dystrophy: A neglectedcause of mental retardation

1966 • 48 citations

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

1979 • 48 citations

Myotonic Dystrophy and Pregnancy

1986 • 43 citations

Genetic heterogeneity for dystrophia myotonica.

1972 • 38 citations

Hydrops and pleural effusions in congenital myotonic dystrophy

1988 • 35 citations

VARIANTS OF MYOTONIC DYSTROPHY IN PRE-ADOLESCENT LIFE (THE SYNDROME OF MYOTONIC DYSEMBRYOPLASIA)

1966 • 31 citations

The search for mitochondrial inheritance of human diseases

1985 • 28 citations

Mitochondrial DNA and genetic disease

1992 • 26 citations

Clinical evidence for heterogeneity in myotonic dystrophy.

1982 • 24 citations

Risk estimates for neonatal myotonic dystrophy.

1984 • 19 citations

Thin ribs in neonatal myotonic dystrophy

1975 • 19 citations

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

1983 • 15 citations

PREGNANCY IN MYOTONICA DYSTROPHIA

1958 • 14 citations

Mitochondrial DNA and genetic disease.

1988 • 11 citations

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

1981 • 9 citations

Cystinuria with congenital myotonic dystrophy

1987 • 9 citations

Myotonic dystrophy: limited electromyo‐graphic abnormalities in 2 definite cases

1983 • 8 citations

Neonatal respiratory failure due to myotonic dystrophy.

1975 • 6 citations

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

1983 • 5 citations

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

1985 • 3 citations

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

1985 • 2 citations

Deleted Work

1955 • 0 citations