[cite web | title = Entrez Gene: TMEM67 transmembrane protein 67| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=91147| accessdate = ] ] PBB_Summary
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References
Further reading
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*cite journal | author=Khaddour R, Smith U, Baala L, "et al." |title=Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online. |journal=Hum. Mutat. |volume=28 |issue= 5 |pages= 523-4 |year= 2007 |pmid= 17397051 |doi= 10.1002/humu.9489
*cite journal | author=Consugar MB, Kubly VJ, Lager DJ, "et al." |title=Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3. |journal=Hum. Genet. |volume=121 |issue= 5 |pages= 591-9 |year= 2007 |pmid= 17377820 |doi= 10.1007/s00439-007-0341-3
*cite journal | author=Dawe HR, Smith UM, Cullinane AR, "et al." |title=The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. |journal=Hum. Mol. Genet. |volume=16 |issue= 2 |pages= 173-86 |year= 2007 |pmid= 17185389 |doi= 10.1093/hmg/ddl459
*cite journal | author=Baala L, Romano S, Khaddour R, "et al." |title=The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome. |journal=Am. J. Hum. Genet. |volume=80 |issue= 1 |pages= 186-94 |year= 2007 |pmid= 17160906 |doi= 10.1086/510499
*cite journal | author=Smith UM, Consugar M, Tee LJ, "et al." |title=The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat. |journal=Nat. Genet. |volume=38 |issue= 2 |pages= 191-6 |year= 2006 |pmid= 16415887 |doi= 10.1038/ng1713
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Morgan NV, Gissen P, Sharif SM, "et al." |title=A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24. |journal=Hum. Genet. |volume=111 |issue= 4-5 |pages= 456-61 |year= 2002 |pmid= 12384791 |doi= 10.1007/s00439-002-0817-0
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