Find link

language:

jump to random article

Find link is a tool written by Edward Betts.

searching for Primary ciliary dyskinesia 11 found (62 total)

alternate case: primary ciliary dyskinesia

DNAH5 (849 words) [view diff] exact match in snippet view article find links to article

left-right asymmetry.3 Mutations of the DNAH5 gene are linked to primary ciliary dyskinesia, an autosomal recessive disorder.4 This X-linked disorder is characterized
DNAI1 (802 words) [view diff] exact match in snippet view article find links to article
abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia (PCD) and Kartagener syndrome. The DNAi1 gene (axonemal dynein
DNAH1 (469 words) [view diff] exact match in snippet view article find links to article
Naturally occurring mutations in this gene are associated with primary ciliary dyskinesia and multiple morphological anomalies of the flagella that result
DNAH9 (617 words) [view diff] exact match in snippet view article find links to article
sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia". Genomics. 72 (1): 21–33. doi:10.1006/geno.2000.6462. hdl:2123/16163
CCDC40 (gene) (424 words) [view diff] case mismatch in snippet view article
Smith RJ, Stephens K, Zariwala MA, Knowles MR, Leigh MW (1993). "Primary Ciliary Dyskinesia". PMID 20301301. Cite journal requires |journal= (help) Blanchon
SPEF2 (572 words) [view diff] exact match in snippet view article find links to article
SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia". Biology of Reproduction. 85 (4): 690–701. doi:10.1095/biolreprod
Mimiviridae (2,110 words) [view diff] case mismatch in snippet view article find links to article
2020). "Pulmonary Infection Related to Mimivirus in Patient with Primary Ciliary Dyskinesia". Emerging Infectious Diseases. 26 (10): 2524–2526. doi:10.3201/eid2610
FOXJ1 (2,069 words) [view diff] exact match in snippet view article find links to article
deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)". Cytogenetics and Cell Genetics. 90 (1–2): 119–22. doi:10
Orange ribbon (1,569 words) [view diff] case mismatch in snippet view article find links to article
United States, the orange ribbon has become a support color for Primary Ciliary Dyskinesia (PCD), a rare lung disease Gun violence protests At-risk animal
Strømme syndrome (2,717 words) [view diff] exact match in snippet view article find links to article
jejunal atresia with microcephaly and ocular anomalies, (formerly) primary ciliary dyskinesia 31 (CILD31) Female infant with Strømme syndrome showing microcephaly
2021 New Year Honours (23,342 words) [view diff] case mismatch in snippet view article find links to article
Copeland. Lately Chair, Primary Ciliary Dyskinesia Family Support Group. For services to Raising Awareness of Primary Ciliary Dyskinesia. (Milton Keynes, Buckinghamshire)