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:


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