Original | CFTR gene on chromosome 7 produce mucus which is unusually thick and sticky clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts Heterozygous carriers who possess one normal allele will not develop disease symptoms |
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Title | Cystic fibrosis is an autosomal recessive disorder caused by a mutation to the ... Individuals with cystic fibrosis will ... which ... |
Settings | 1,1,0 | n,n,n,n |
Text1 | CFTR gene on chromosome 7 ... ... ... |
Text2 | CFTR gene on chromosome 7 produce mucus which is unusually thick and sticky ... ... |
Text3 | ... produce mucus which is unusually thick and sticky clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts ... |
Text4 | ... ... clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts Heterozygous carriers who possess one normal allele will not develop disease symptoms |
Full | CFTR gene on chromosome 7 produce mucus which is unusually thick and sticky clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts Heterozygous carriers who possess one normal allele will not develop disease symptoms |
Tags: 3_4_inheritance, cystic_fibrosis
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