about
Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5qEvidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1BThe genetic status of mothers of isolated cases of Duchenne muscular dystrophy.Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short armSEVERE MUSCULAR DYSTROPHY IN GIRLSCalculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom.Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy.Genetic counselling in facioscapulohumeral muscular dystrophyOn the heredity of retinitis pigmentosa.No sex difference in mutations rates of Duchenne muscular dystrophy.A population study of adult onset limb-girdle muscular dystrophyA simple method for calculating risks before DNA analysis.Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7X-chromosome mosaicism in females with muscular dystrophy.Mutation rate in Duchenne type of muscular dystrophy.Genetic-epidemiological studies in progressive muscular dystrophy.Mutation rate in Duchenne muscular dystrophy.Creatine phosphokinase levels in the newborn and their use in screening for Duchenne muscular dystrophy.On the power to detect differences between male and female mutation rates for Duchenne muscular dystrophy, using classical segregation analysis and restriction fragment length polymorphisms.Answer to criticism of Morton and LalouelTransition matrices with mutationThe detection of major genes under additive continuous variationThe effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B.The effects of parental consanguinity and inbreeding in Hirado, Japan. V. Summary and interpretation.High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesEvidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.Prevalence of Duchenne and Becker muscular dystrophies in the United States.Discrimination of genetic entities in muscular dystrophySerum enzymes and genetic carriers in muscular dystrophy.Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase DeterminationThe mutational load due to detrimental genes in man.Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates.Genetics of spherocytosisESTIMATION OF PREVALENCE UNDER INCOMPLETE SELECTION.RECESSIVE GENES IN SEVERE MENTAL DEFECTRespiratory involvement in inherited primary muscle conditions.Segregation analysisVariability of incidence and clinical manifestation of mouse hereditary muscular dystrophy on heterogeneous genetic backgrounds.Mutation rates of the abnormal hemoglobin genes.
P2860
Q24670253-CB3F8AF4-D295-4F2E-8440-FFAB3E4FE5CEQ24670624-54EE5BF9-62D5-41B5-B70B-CD8322F58B2BQ29041262-C2D29D11-5AF7-4FC0-BD24-1349F405322FQ30443071-48A91023-7931-4E1B-A49A-EE2A56EE24C6Q33584511-1A845067-150E-485E-A771-0F0A5FE716EFQ33584865-05365500-C078-4CCC-ACB9-110F20EB168AQ33588153-491EBABA-45C6-406C-A326-A6F9B393769AQ33588259-27AC660A-90F9-4CA6-B207-3DD137404BDFQ33597601-6DC42A18-A0FB-480A-B640-E0B4B08B5B5EQ33641994-0AE378D3-2542-482D-9730-DB6BDA4C2310Q33667794-8421F563-633B-4991-AF75-9914C366F98CQ33672061-292E5971-A721-4076-B128-3DAA3C21AD64Q33681920-0458D266-612E-47AF-A9AF-7EDA37AB5BA5Q34388920-54AB6BD5-23CA-4F7B-8FBE-FC08625379B8Q34427092-ECDFECD0-F70A-4EE5-A0E8-51B41C1A67B9Q34634019-92E98511-B4F1-45C7-90AF-EA4A34765145Q34634134-8B01EFDA-9F62-4035-8A0A-88BFB0814BD1Q34634939-338DF6C2-7547-4D7D-8F5C-357A2FB352DEQ34987790-57007D6C-A1B0-421C-973C-8B799D8BC7ADQ35200995-C5E03C94-5820-4F53-842E-414193AF0AF3Q35202160-16E00654-2EDA-463B-9688-9B1216CDAF58Q35203672-D7EC0E40-BEA4-42C6-9ABD-0A02DFBE6B7CQ35231226-D62EE082-D0B2-4259-8901-FF63E00EE5F2Q35231697-C39FD614-1CC5-48FD-B6DA-3433B91F5CBAQ35569292-2BC96E7C-20C7-444D-8D6D-140383AA2DB9Q35643770-CA6A28B3-B1A7-4B6E-A2B5-F7A638CC8E77Q35644058-0BBAC435-3645-4766-B95B-3FF84E2E9778Q35770545-EFA3D49A-BD4A-4465-8E2E-5DB04EBECC6EQ35911785-AD68D500-9E32-4FD5-81F3-8E71D7243A71Q35911811-04642744-8B9E-4658-B070-D190EEB87955Q35912145-61631969-32B7-48AC-BEE4-8D4D60C0A2E5Q35912221-840256F1-C713-4A75-AD1B-E9CBA9422D32Q35912230-01345FF7-6D23-4C64-B238-BFBFBBDFF33CQ35912252-09ADA75C-F8AB-421F-A4D3-84FBC0FCC28DQ35912941-AED5BF1F-9FC3-4723-8C68-8F29E8186C0CQ35912946-A309152E-77BD-49F9-A2A2-554A1F27A01FQ36596271-84D3ABCF-781E-49B3-B29D-2B32349048D3Q41525462-53584DFA-4992-4E91-87F0-7DF4798A1F23Q41829696-6286FC03-4063-4966-9EB7-F6E494AA769EQ42433347-3A3AF2CA-0FA9-45EC-8235-401B594D95FE
P2860
description
1959 nî lūn-bûn
@nan
1959年の論文
@ja
1959年論文
@yue
1959年論文
@zh-hant
1959年論文
@zh-hk
1959年論文
@zh-mo
1959年論文
@zh-tw
1959年论文
@wuu
1959年论文
@zh
1959年论文
@zh-cn
name
Formal genetics of muscular dystrophy.
@ast
Formal genetics of muscular dystrophy.
@en
type
label
Formal genetics of muscular dystrophy.
@ast
Formal genetics of muscular dystrophy.
@en
prefLabel
Formal genetics of muscular dystrophy.
@ast
Formal genetics of muscular dystrophy.
@en
P2860
P1476
Formal genetics of muscular dystrophy.
@en
P2093
P2860
P304
P407
P577
1959-12-01T00:00:00Z