<--- Back to Details
First PageDocument Content
Muscular dystrophy / Classical genetics / Congenital muscular dystrophy / Microsatellite / Chromosome 1 / Ataxia telangiectasia / Walker–Warburg syndrome / Haplotype / Genetic linkage / Genetics / Health / Biology
Date: 2010-05-05 13:28:49
Muscular dystrophy
Classical genetics
Congenital muscular dystrophy
Microsatellite
Chromosome 1
Ataxia telangiectasia
Walker–Warburg syndrome
Haplotype
Genetic linkage
Genetics
Health
Biology

s00439[removed]4ca-web[removed]

Add to Reading List

Source URL: curecmd.org

Download Document from Source Website

File Size: 231,87 KB

Share Document on Facebook

Similar Documents

Congenital disorders / Keratoderma / Walker–Warburg syndrome / Hypoplasia / Hypotonia / Rosselli-Gulienetti syndrome / Arthrogryposis / DiGeorge syndrome / Ectrodactyly–ectodermal dysplasia–cleft syndrome / Health / Syndromes / Rare diseases

The human disease network ′ A-LProc Natl Acad Sci USA 104:Goh K-I, Cusick ME, Valle D, Childs B, Vidal M, Barabasi Urolithiasise Caffey

DocID: 14S6x - View Document

Rare diseases / Respiratory therapy / Motor neurone disease / Congenital disorders / Duchenne muscular dystrophy / Spinal muscular atrophies / Congenital muscular dystrophy / Pulmonary function testing / Walker–Warburg syndrome / Health / Medicine / Muscular dystrophy

Journal http://jcn.sagepub.com/ of Child Neurology Consensus Statement on Standard of Care for Congenital Muscular Dystrophies Ching H. Wang, Carsten G. Bonnemann, Anne Rutkowski, Thomas Sejersen, Jonathan Bellini, Vanes

DocID: 11ZL1 - View Document

Congenital disorders / Keratoderma / Walker–Warburg syndrome / Hypoplasia / Hypotonia / Rosselli-Gulienetti syndrome / Arthrogryposis / DiGeorge syndrome / Ectrodactyly–ectodermal dysplasia–cleft syndrome / Health / Syndromes / Rare diseases

The human disease network ′ A-L[removed]Proc Natl Acad Sci USA 104:[removed]Goh K-I, Cusick ME, Valle D, Childs B, Vidal M, Barabasi Urolithiasise Caffey

DocID: XDko - View Document

Medical genetics / Congenital muscular dystrophy / Dystroglycan / Walker–Warburg syndrome / Limb-girdle muscular dystrophy / POMGNT1 / Kevin Campbell / Myopathy / Fukuyama congenital muscular dystrophy / Muscular dystrophy / Health / Genetic genealogy

Researchers identify new form of muscular dystrophy

DocID: RsDZ - View Document

Miller–Dieker syndrome / Aicardi syndrome / Joubert syndrome / Trisomy 8 / Lissencephaly / Pachygyria / Down syndrome / Noonan syndrome / Patau syndrome / Health / Syndromes / Walker–Warburg syndrome

3_Established_Conditions_list

DocID: JZuc - View Document