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Out, out damn spot, or the demise of the Mongolian spot.
Lin AE, Feingold M, Siegel B. Lin AE, et al. Among authors: feingold m. Am J Dis Child. 1993 Jul;147(7):714. doi: 10.1001/archpedi.1993.02160310016004. Am J Dis Child. 1993. PMID: 8322733 No abstract available.
Telediagnostic conferencing.
Feingold M, Frias J, Lin AE, Schaefer GB, Horwitz M. Feingold M, et al. Am J Dis Child. 1993 Nov;147(11):1196. doi: 10.1001/archpedi.1993.02160350070010. Am J Dis Child. 1993. PMID: 8237914 No abstract available.
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.
Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Goodman FR, et al. Among authors: feingold m. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 Jun 5. Am J Hum Genet. 2000. PMID: 10839976 Free PMC article.
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.
Hanks S, Adams S, Douglas J, Arbour L, Atherton DJ, Balci S, Bode H, Campbell ME, Feingold M, Keser G, Kleijer W, Mancini G, McGrath JA, Muntoni F, Nanda A, Teare MD, Warman M, Pope FM, Superti-Furga A, Futreal PA, Rahman N. Hanks S, et al. Among authors: feingold m. Am J Hum Genet. 2003 Oct;73(4):791-800. doi: 10.1086/378418. Epub 2003 Aug 21. Am J Hum Genet. 2003. PMID: 14508707 Free PMC article.
Down syndrome and systemic lupus erythematosus.
Feingold M, Schneller S. Feingold M, et al. Clin Genet. 1995 Nov;48(5):277. doi: 10.1111/j.1399-0004.1995.tb04106.x. Clin Genet. 1995. PMID: 8825610 No abstract available.
Marital status of Down syndrome parents.
Feingold M. Feingold M. Arch Pediatr Adolesc Med. 1996 Jun;150(6):650-1. doi: 10.1001/archpedi.1996.02170310084018. Arch Pediatr Adolesc Med. 1996. PMID: 8646321 No abstract available.
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis.
de Munnik SA, Bicknell LS, Aftimos S, Al-Aama JY, van Bever Y, Bober MB, Clayton-Smith J, Edrees AY, Feingold M, Fryer A, van Hagen JM, Hennekam RC, Jansweijer MC, Johnson D, Kant SG, Opitz JM, Ramadevi AR, Reardon W, Ross A, Sarda P, Schrander-Stumpel CT, Schoots J, Temple IK, Terhal PA, Toutain A, Wise CA, Wright M, Skidmore DL, Samuels ME, Hoefsloot LH, Knoers NV, Brunner HG, Jackson AP, Bongers EM. de Munnik SA, et al. Among authors: feingold m. Eur J Hum Genet. 2012 Jun;20(6):598-606. doi: 10.1038/ejhg.2011.269. Epub 2012 Feb 15. Eur J Hum Genet. 2012. PMID: 22333897 Free PMC article.
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects.
Boyle L, Wamelink MMC, Salomons GS, Roos B, Pop A, Dauber A, Hwa V, Andrew M, Douglas J, Feingold M, Kramer N, Saitta S, Retterer K, Cho MT, Begtrup A, Monaghan KG, Wynn J, Chung WK. Boyle L, et al. Among authors: feingold m. Am J Hum Genet. 2016 Jun 2;98(6):1235-1242. doi: 10.1016/j.ajhg.2016.03.030. Am J Hum Genet. 2016. PMID: 27259054 Free PMC article.
402 results