Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
about
Molecular genetics and genetic testing in myotonic dystrophy type 1.Moebius syndromeMendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.Genetics of Möbius syndrome.Genetic aspects of hereditary motor and sensory neuropathy (types I and II)Clinical evidence for heterogeneity in myotonic dystrophyA case of paternally inherited congenital myotonic dystrophy.Paternal transmission of congenital myotonic dystrophyPaternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.Genetic heterogeneity for dystrophia myotonica.Congenital myotonic dystrophy in Britain. II. Genetic basisCongenital myotonic dystrophy in Britain. I. Clinical aspects.Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reportsAnticipation in myotonic dystrophy: new light on an old problem.Genetic risks for children of women with myotonic dystrophy.Homozygote for Huntington diseaseLens epithelial changes and mutated gene expression in patients with myotonic dystrophy.Parental age effects, but no evidence for an intrauterine effect in the transmission of myotonic dystrophy type 1.Congenital myotonic dystrophy: respiratory function at birth determines survival.The future of genetic epidemiology.Allelic instability in mitosis: a unified model for dominant disordersDystrophia myotonica and pregnancy--an instructive case.Anticipation in hereditary disease: the history of a biomedical concept.CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic DystrophyMyotonia congenita (Thomsen's disease). Early diagnosis in infancy.Evaluation of information-processing speed and neuropsychological functioning in patients with myotonic dystrophy.Neonatal respiratory failure due to myotonic dystrophy.Centronuclear myopathy: clinical and pathologic features. Unlike early onset myotonic dystrophy, this condition is not associated with mental retardation or clinical or electric evidences of myotonia.Preimplantation Genetic Diagnosis for Myotonic Dystrophy Type 1 and Analysis of the Effect of the Disease on the Reproductive Outcome of the Affected Female Patients.Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms.Core Clinical Phenotypes in Myotonic Dystrophies.Paternal transmission of congenital myotonic dystrophy.
P2860
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P2860
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
description
1972 nî lūn-bûn
@nan
1972 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1972 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
name
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@ast
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@en
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@nl
type
label
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@ast
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@en
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@nl
prefLabel
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@ast
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@en
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@nl
P1433
P1476
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor.
@en
P2093
P356
10.1016/S0140-6736(72)91548-6
P407
P577
1972-07-01T00:00:00Z