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Page 1
Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome.
Stewart DR, Huang A, Faravelli F, Anderlid BM, Medne L, Ciprero K, Kaur M, Rossi E, Tenconi R, Nordenskjöld M, Gripp KW, Nicholson L, Meschino WS, Capua E, Quarrell OW, Flint J, Irons M, Giampietro PF, Schowalter DB, Zaleski CA, Malacarne M, Zackai EH, Spinner NB, Krantz ID. Stewart DR, et al. Among authors: schowalter db. Am J Med Genet A. 2004 Aug 1;128A(4):340-51. doi: 10.1002/ajmg.a.30136. Am J Med Genet A. 2004. PMID: 15264279
Congenital and idiopathic scoliosis: clinical and genetic aspects.
Giampietro PF, Blank RD, Raggio CL, Merchant S, Jacobsen FS, Faciszewski T, Shukla SK, Greenlee AR, Reynolds C, Schowalter DB. Giampietro PF, et al. Among authors: schowalter db. Clin Med Res. 2003 Apr;1(2):125-36. doi: 10.3121/cmr.1.2.125. Clin Med Res. 2003. PMID: 15931299 Free PMC article. Review.
Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome.
Giampietro PF, Schowalter DB, Merchant S, Campbell LR, Swink T, Roa BB. Giampietro PF, et al. Among authors: schowalter db. Childs Nerv Syst. 2006 Mar;22(3):320-4. doi: 10.1007/s00381-005-1155-z. Epub 2005 May 5. Childs Nerv Syst. 2006. PMID: 15875198
Gene therapy: a status report.
Schowalter DB, Kay MA. Schowalter DB, et al. Pediatr Ann. 1997 Sep;26(9):562-8. doi: 10.3928/0090-4481-19970901-12. Pediatr Ann. 1997. PMID: 9302719 No abstract available.
25 results