About: On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies

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scientific article published on 01 August 1955

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1955 (uk) im August 1955 veröffentlichter wissenschaftlicher Artikel (de) 1955 թվականի օգոստոսի 1-ին հրատարակված գիտական հոդված (hy) artículu científicu espublizáu n'agostu de 1955 (ast) scientific article published on 01 August 1955 (en)
publication date	wds:Q73785997-5748A9A3-B53B-45A6-AEF5-8A1B925C4A5B
publication date	1955-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73785997-17B032C3-E34B-4F9E-9474-66D4433A6157 wds:Q73785997-34AB8894-274C-4A30-BC66-0689327904A0 wds:Q73785997-AE9BD286-0C74-419F-9C6F-435BBCB899F0
author name string	R R RACE J N WALTON U PHILIP
rdfs:label	On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (en) On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (nl)
skos:prefLabel	On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (en) On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (nl)
name	On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (en) On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (nl)
title	wds:Q73785997-FB31BC06-8DF5-4AC3-A9A8-AE4EC9DE293B
title	On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies (en)
page(s)	wds:Q73785997-FC7BDA51-3B8A-4B84-B5BD-F2DBD28151A7
page(s)	1-38
instance of	wds:Q73785997-214B8A23-BA58-46A1-BF6B-BB782B8CBC3E
instance of	scholarly article
main subject	wds:Q73785997-CD8FB0C1-096D-4800-8F56-B8D8610245D2
main subject	muscular dystrophy
PubMed ID	wds:Q73785997-0F6936D1-E88C-4D2E-B44D-C46DA7F2E231
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13249224
PubMed ID	13249224
published in	wds:Q73785997-D28D210B-AA0C-4767-BE4B-3C0C00EBB5E8
published in	Annals of Human Genetics
issue	wds:Q73785997-11B61523-D491-4845-B101-B6D765F36EE3
volume	wds:Q73785997-2A24BDC3-C43E-434D-AD7A-A721452CDADC
issue	1
volume	20
DOI	wds:Q73785997-CCA94F8F-934F-4360-8FBE-9A53275AB843
DOI	http://dx.doi.org/10.1111/J.1469-1809.1955.TB01274.X
DOI	10.1111/J.1469-1809.1955.TB01274.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73785997
is cites work of	Formal genetics of muscular dystrophy Population frequencies of inherited neuromuscular diseases—A world survey Unusual type of benign x-linked muscular dystrophy Serum enzymes and genetic carriers in muscular dystrophy. Selection at the ABO locus. Incidence of Duchenne muscular dystrophy in New South Wales and Australian Capital Territory Mutation rate in Duchenne type of muscular dystrophy The Genetic Relationship of Progressive Muscular Dystrophy (Duchenne Type) and Mental Retardation Pseudohypertrophic Muscular Dystrophy of Childhood: An epidemiological survey in Victoria Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention MUSCULAR DYSTROPHY (DUCHENNE) IN A GIRL WITH TURNER'S SYNDROME. Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination A biochemical study of certain skeletal muscle constituents in human progressive muscular dystrophy The incidence of necrosis of muscle fibers in Duchenne type muscular dystrophy. Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy Becker-type muscular dystrophy SOME DISEASES OF MUSCLE Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands Carrier Detection in Duchenne Muscular Dystrophy Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man. Aminoglycoside-induced mutation suppression (stop codon readthrough) as a therapeutic strategy for Duchenne muscular dystrophy Myopathy in sheep; its relationship to scrapie and to dermatomyositis and muscular dystrophy A population study of adult onset limb-girdle muscular dystrophy Pedigree testing in duchenne muscular dystrophy The golden retriever model of Duchenne muscular dystrophy The Genetics of Muscular Dystrophy A probable sex difference in some mutation rates. CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. I. SERUM ENZYMES IN PROGRESSIVE MUSCULAR DYSTROPHY (TYPE I, II, IIIA) Some studies of the Duchenne and autosomal recessive types of muscular dystrophy Myocardial infarction in progressive muscular dystrophy Autosomal recessive muscular dystrophy in Manitoba Hutterites* Duchenne muscular dystrophy. A population study Epidemiology of Duchenne muscular dystrophy in the province of Turin Are the MN blood group maintained by selection? Serum enzyme studies in inherited disease of skeletal muscle New data on the genetics and classification of muscular dystrophies A new variant phenotype of the group-specific component (Gc) found in a Japanese family Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE The frequency of conditions due to mutant genes of large effect SEVERE MUSCULAR DYSTROPHY IN GIRLS The X chromosome of man The female carrier of Duchenne muscular dystrophy. The genetic status of mothers of isolated cases of Duchenne muscular dystrophy. The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups Diagnosis of female carriers of Duchenne's progressive muscular dystrophy using discriminative analysis of various serum enzyme activities Contribution on the study of pseudohypertrophic muscular dystrophies. II. Pseudohypertrophic muscular dystrophies in females Facioscapulohumeral muscular dystrophy concentrated in the village Cullar, Nevşehir, Turkey Muscular dystrophy in three pairs of twins Bibliography of Human Genetics
is cites work of	wds:Q33668069-1DF87BBF-E5C1-4BD8-84F9-48F185C269BB wds:Q33585048-D827ADC9-D7B5-4EE1-94F1-18AE178581A7 wds:Q69024134-B7E1F7B9-0F0B-42EB-9EDD-442BFB10F4BC wds:Q76942277-843C867F-A1FB-402B-8A5E-B740C3631E95 wds:Q28266298-1201C607-3CC0-4C6A-B7D7-9CC3187D234F wds:Q33588259-9A2CB6AC-D214-4710-B2B3-DB9595A1F75B wds:Q35911789-8F57B393-D4DA-4026-A81C-F821782DDCC1 wds:Q52127108-53B26832-7A2C-4566-9A58-34357D764103

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