Aldahmesh, Mohamed A <br/><br/>
Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example.  [electronic resource] 

 -  American journal of medical genetics. Part A  Feb 2009 
 - 662-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32753  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Base Sequence<br/>Cardiomyopathy, Dilated--genetics<br/>Cell Cycle Proteins<br/>Child<br/>Child, Preschool<br/>Codon, Nonsense<br/>Consanguinity<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Frameshift Mutation<br/>Hearing Loss, Sensorineural--genetics<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Insulin Resistance--genetics<br/>Liver Failure--genetics<br/>Male<br/>Mutation<br/>Obesity--genetics<br/>Proteins--genetics<br/>Renal Insufficiency--genetics<br/>Retinitis Pigmentosa--genetics<br/>Saudi Arabia<br/>Syndrome