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Page 1
Ontogeny of milky spots in the human greater omentum: an immunochemical study.
Krist LF, Koenen H, Calame W, van der Harten JJ, van der Linden JC, Eestermans IL, Meyer S, Beelen RH. Krist LF, et al. Among authors: van der harten jj. Anat Rec. 1997 Nov;249(3):399-404. doi: 10.1002/(SICI)1097-0185(199711)249:3<399::AID-AR11>3.0.CO;2-J. Anat Rec. 1997. PMID: 9372174 Free article.
An unusual cause of recurrent fever.
Los H, Schramel FM, van der Harten JJ, Golding RP, Postmus PE. Los H, et al. Among authors: van der harten jj. Eur Respir J. 1997 Feb;10(2):504-7. doi: 10.1183/09031936.97.10020504. Eur Respir J. 1997. PMID: 9042658 Free article. No abstract available.
A family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans.
Superti-Furga A, Hästbacka J, Rossi A, van der Harten JJ, Wilcox WR, Cohn DH, Rimoin DL, Steinmann B, Lander ES, Gitzelmann R. Superti-Furga A, et al. Among authors: van der harten jj. Ann N Y Acad Sci. 1996 Jun 8;785:195-201. doi: 10.1111/j.1749-6632.1996.tb56259.x. Ann N Y Acad Sci. 1996. PMID: 8702127 Review. No abstract available.
Early second-trimester diagnosis of sirenomelia.
van Zalen-Sprock MM, van Vugt JM, van der Harten JJ, van Geijn HP. van Zalen-Sprock MM, et al. Among authors: van der harten jj. Prenat Diagn. 1995 Feb;15(2):171-7. doi: 10.1002/pd.1970150211. Prenat Diagn. 1995. PMID: 7784370
Phenotypically dissimilar hypophosphatasia in two sibships.
Macfarlane JD, Kroon HM, van der Harten JJ. Macfarlane JD, et al. Among authors: van der harten jj. Am J Med Genet. 1992 Jan 1;42(1):117-21. doi: 10.1002/ajmg.1320420124. Am J Med Genet. 1992. PMID: 1308350
33 results