[HTML][HTML] Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge
M Albalawi, A Al-Shamrani, AS Mohamed… - The American Journal …, 2024 - ncbi.nlm.nih.gov
Objective: Unknown etiology Background: Primary ciliary dyskinesia (PCD) is a rare
autosomal recessive disease that can present at different ages with different phenotypes …
autosomal recessive disease that can present at different ages with different phenotypes …
Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge.
M Albalawi, A Al-Shamrani… - American Journal of …, 2024 - search.ebscohost.com
Abstract Objective: Unknown etiology Background: Primary ciliary dyskinesia (PCD) is a rare
autosomal recessive disease that can present at different ages with different phenotypes …
autosomal recessive disease that can present at different ages with different phenotypes …
Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge
M Albalawi, A Al-Shamrani… - … journal of case …, 2024 - pubmed.ncbi.nlm.nih.gov
BACKGROUND Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease that
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge.
M Albalawi, A Al-Shamrani, AS Mohamed… - The American Journal …, 2024 - europepmc.org
BACKGROUND Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease that
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
[PDF][PDF] Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge
Am J Case Rep, 2024 - scienceopen.com
Background: Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease that
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge.
M Albalawi, A Al-Shamrani, AS Mohamed… - The American Journal …, 2024 - europepmc.org
BACKGROUND Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease that
can present at different ages with different phenotypes. Missed and delayed diagnoses are …
can present at different ages with different phenotypes. Missed and delayed diagnoses are …