Shahid, Muhammad <br/><br/>
Screening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations.  [electronic resource] 

 -  Congenital anomalies  Jan 2020 
 - 32-39 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1741-4520 
<br/><br/><label>Standard No.: </label>10.1111/cga.12331  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>DNA Mutational Analysis<br/>Fanconi Anemia--epidemiology<br/>Fanconi Anemia Complementation Group A Protein--genetics<br/>Female<br/>Genotype<br/>Homozygote<br/>Humans<br/>Introns--genetics<br/>Male<br/>Mutation--genetics<br/>Pakistan--epidemiology