http://www.ncbi.nlm.nih.gov/genome/guide/HsChrX.shtml
Adrenoleukodystrophy Duchenne Muscular_dystrophy Lowe Syndrome Norrie Disease Rett_syndrome See OMIM or Genes and Disease for additional examples
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr2.shtml
for Human Chr. 2 Chromosome 2 Disease Genes Some diseases associated with chromosome 2 mutations Alstrom Syndrome Holoprosencephaly 2 Tibial Muscular_dystrophy Autosomal Recessive Deafness
-9 Limb Girdle Muscular_dystrophy 2b See OMIM
http://www.ncbi.nlm.nih.gov/disease/Muscle.html
Muscle and bone Duchenne muscular_dystrophy Ellis-van_creveld_syndrome Marfan_syndrome Myotonic_dystrophy Spinal muscular_atrophy THE SKELETON provides an anchor point against
. Two diseases that originate through a defect in the muscle_cells themselves are Duchenne muscular_dystrophy (DMD) and myotonic_dystrophy (DM.
http://www.ncbi.nlm.nih.gov:80/entrez/journals/active_providers.html
) Elsevier Science (ES) EMBL Reptile Database (emblrep) Emery-Dreifuss Muscular_dystrophy Mutation Database
http://www.ncbi.nlm.nih.gov/entrez/Omim/allresources.html
The BTKBASE mutation registry for X-Linked agammaglobulinemia The Cystic_fibrosis Mutation Database The Emery-Dreifuss Muscular_dystrophy Mutation
http://www.ncbi.nlm.nih.gov:80/entrez/journals/loprovlink.html
Taxonomy Emery-Dreifuss Muscular_dystrophy Mutation Database (EMD: