Genetic counselling in X-linked muscular dystrophy. - National Genomics Data Center (CNCB-NGDC)

Advanced Search

Genetic counselling in X-linked muscular dystrophy.

A E Emery

Author Information

PMID: 4185251 DOI: 10.1016/0022-510x(69)90016-1

No abstract text available.

Blood Flow Velocity

Counseling

Creatine Kinase

Electromyography

Female

Genes

Heterozygote

Homozygote

Humans

Immunoelectrophoresis

Isoenzymes

L-Lactate Dehydrogenase

Male

Muscles

Muscular Dystrophies

Potassium

Regional Blood Flow

Sex Chromosomes

Statistics as Topic

gamma-Globulins

Isoenzymes

gamma-Globulins

L-Lactate Dehydrogenase

Creatine Kinase

Potassium

Journal Article

X-linked muscular dystrophy.Genetic counselling in facioscapulohumeral muscular dystrophy.Muscular dystrophy: genetic counselling and family planning.[Genetic counselling for Duchenne muscular dystrophy].Gene deletions in X-linked muscular dystrophy.X-linked muscular dystrophy in the dog.Carrier detection in X-linked muscular dystrophy.Genetic counselling in lethal X-linked disorders.Canine X-linked muscular dystrophy: morphologic lesions.[X-linked muscular dystrophy: is prevention possible?].

Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers.Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases.The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.Population data on benign and severe forms of X-linked muscular dystrophy.Serum creatine kinase studies in the detection of carriers of Duchenne dystrophy.Serum creatine kinase levels in normal females.A genetic study of Duchenne muscular dystrophy in West Midlands.The female carrier of Duchenne muscular dystrophy.Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.