Daniels, R J <br/><br/>
Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.  [electronic resource] 

 -  Human molecular genetics  Feb 2001 
 - 339-52 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/10.4.339  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Animals<br/>Asthma--genetics<br/>Base Composition<br/>Bipolar Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 16--chemistry<br/>CpG Islands--genetics<br/>Epilepsy--genetics<br/>Female<br/>Genetic Linkage--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mice<br/>Monosomy<br/>Phenotype<br/>Physical Chromosome Mapping<br/>Polycystic Kidney, Autosomal Dominant--genetics<br/>Recombination, Genetic<br/>Sequence Analysis, DNA<br/>Syndrome<br/>Telomere--chemistry<br/>Tuberous Sclerosis--genetics<br/>alpha-Thalassemia--genetics