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Cleidocranial dysplasia in mice.

Mundlos S, Huang LF, Selby P, Olsen BR. Mundlos S, et al. Ann N Y Acad Sci. 1996 Jun 8;785:301-2. doi: 10.1111/j.1749-6632.1996.tb56290.x. Ann N Y Acad Sci. 1996. PMID: 8702161 No abstract available.

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Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13.

Muragaki Y, Mundlos S, Upton J, Olsen BR. Muragaki Y, et al. Among authors: mundlos s. Science. 1996 Apr 26;272(5261):548-51. doi: 10.1126/science.272.5261.548. Science. 1996. PMID: 8614804

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Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development-transcription factors and signaling pathways.

Mundlos S, Olsen BR. Mundlos S, et al. FASEB J. 1997 Feb;11(2):125-32. doi: 10.1096/fasebj.11.2.9039954. FASEB J. 1997. PMID: 9039954 Review.

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Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis.

Mundlos S, Olsen BR. Mundlos S, et al. FASEB J. 1997 Mar;11(4):227-33. FASEB J. 1997. PMID: 9068611 Review.

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Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant mice.

Huang LF, Fukai N, Selby PB, Olsen BR, Mundlos S. Huang LF, et al. Among authors: mundlos s. Dev Dyn. 1997 Sep;210(1):33-40. doi: 10.1002/(SICI)1097-0177(199709)210:1<33::AID-AJA4>3.0.CO;2-2. Dev Dyn. 1997. PMID: 9286593 Free article.

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Severe cleidocranial dysplasia can mimic hypophosphatasia.

Unger S, Mornet E, Mundlos S, Blaser S, Cole DE. Unger S, et al. Among authors: mundlos s. Eur J Pediatr. 2002 Nov;161(11):623-6. doi: 10.1007/s00431-002-0978-9. Epub 2002 Jun 28. Eur J Pediatr. 2002. PMID: 12424591

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A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.

Gensure RC, Mäkitie O, Barclay C, Chan C, Depalma SR, Bastepe M, Abuzahra H, Couper R, Mundlos S, Sillence D, Ala Kokko L, Seidman JG, Cole WG, Jüppner H. Gensure RC, et al. Among authors: mundlos s. J Clin Invest. 2005 May;115(5):1250-7. doi: 10.1172/JCI22760. J Clin Invest. 2005. PMID: 15864348 Free PMC article.

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Up-regulation of RUNX2 in acute myeloid leukemia in a patient with an inherent RUNX2 haploinsufficiency and cleidocranial dysplasia.

Schnerch D, Lausch E, Becker H, Felthaus J, Pfeifer D, Mundlos S, Engelhardt M, Schwabe M, Wäsch R. Schnerch D, et al. Among authors: mundlos s. Leuk Lymphoma. 2014 Aug;55(8):1930-2. doi: 10.3109/10428194.2013.855310. Epub 2014 Feb 24. Leuk Lymphoma. 2014. PMID: 24138303 No abstract available.

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The role of sonic hedgehog in vertebrate development.

Weed M, Mundlos S, Olsen BR. Weed M, et al. Among authors: mundlos s. Matrix Biol. 1997 May;16(2):53-8. doi: 10.1016/s0945-053x(97)90072-x. Matrix Biol. 1997. PMID: 9205942 Review.

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Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.

Otto F, Kanegane H, Mundlos S. Otto F, et al. Among authors: mundlos s. Hum Mutat. 2002 Mar;19(3):209-16. doi: 10.1002/humu.10043. Hum Mutat. 2002. PMID: 11857736 Review.

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