Cass DT - Search Results

1

A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.

Angrist M, Kauffman E, Slaugenhaupt SA, Matise TC, Puffenberger EG, Washington SS, Lipson A, Cass DT, Reyna T, Weeks DE, et al. Angrist M, et al. Among authors: cass dt. Nat Genet. 1993 Aug;4(4):351-6. doi: 10.1038/ng0893-351. Nat Genet. 1993. PMID: 8401581

2

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.

Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys CH, Cass DT, Chakravarti A. Angrist M, et al. Among authors: cass dt. Hum Mol Genet. 1995 May;4(5):821-30. doi: 10.1093/hmg/4.5.821. Hum Mol Genet. 1995. PMID: 7633441

3

Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.

Mowat DR, Croaker GD, Cass DT, Kerr BA, Chaitow J, Adès LC, Chia NL, Wilson MJ. Mowat DR, et al. Among authors: cass dt. J Med Genet. 1998 Aug;35(8):617-23. doi: 10.1136/jmg.35.8.617. J Med Genet. 1998. PMID: 9719364 Free PMC article.

4

A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease.

Yang GC, Croaker D, Zhang AL, Manglick P, Cartmill T, Cass D. Yang GC, et al. Hum Mol Genet. 1998 Jun;7(6):1047-52. doi: 10.1093/hmg/7.6.1047. Hum Mol Genet. 1998. PMID: 9580670

5

Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locus.

Garcia-Barceló MM, Lau DK, Ngan ES, Leon TY, Liu T, So M, Miao X, Lui VC, Wong KK, Ganster RW, Cass DT, Croaker GD, Tam PK. Garcia-Barceló MM, et al. Among authors: cass dt. Ann Hum Genet. 2008 Mar;72(Pt 2):170-7. doi: 10.1111/j.1469-1809.2007.00403.x. Epub 2007 Dec 12. Ann Hum Genet. 2008. PMID: 18081917 Retracted.

6

Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat.

Ceccherini I, Zhang AL, Matera I, Yang G, Devoto M, Romeo G, Cass DT. Ceccherini I, et al. Among authors: cass dt. Hum Mol Genet. 1995 Nov;4(11):2089-96. doi: 10.1093/hmg/4.11.2089. Hum Mol Genet. 1995. PMID: 8589685

7

Evaluation of the thyroid transcription factor-1 gene (TITF1) as a Hirschsprung's disease locus.

Garcia-Barceló MM, Lau DK, Ngan ES, Leon TY, Liu TT, So MT, Miao XP, Lui VC, Wong KK, Ganster RW, Cass DT, Croaker GD, Tam PK. Garcia-Barceló MM, et al. Among authors: cass dt. Ann Hum Genet. 2007 Nov;71(Pt 6):746-54. doi: 10.1111/j.1469-1809.2007.00384.x. Epub 2007 Jul 19. Ann Hum Genet. 2007. PMID: 17640327

8

Hirschsprung's disease, colonic atresia, and absent hand: a new triad.

Croaker GD, Harvey JG, Cass DT. Croaker GD, et al. Among authors: cass dt. J Pediatr Surg. 1997 Sep;32(9):1368-70. doi: 10.1016/s0022-3468(97)90325-0. J Pediatr Surg. 1997. PMID: 9314266 Review.

9

Congenital central hypoventilation syndrome and Hirschsprung's disease.

Croaker GD, Shi E, Simpson E, Cartmill T, Cass DT. Croaker GD, et al. Among authors: cass dt. Arch Dis Child. 1998 Apr;78(4):316-22. doi: 10.1136/adc.78.4.316. Arch Dis Child. 1998. PMID: 9623393 Free PMC article. Review.

10

Frequency of RET mutations in long- and short-segment Hirschsprung disease.

Seri M, Yin L, Barone V, Bolino A, Celli I, Bocciardi R, Pasini B, Ceccherini I, Lerone M, Kristoffersson U, Larsson LT, Casasa JM, Cass DT, Abramowicz MJ, Vanderwinden JM, Kravcenkiene I, Baric I, Silengo M, Martucciello G, Romeo G. Seri M, et al. Among authors: cass dt. Hum Mutat. 1997;9(3):243-9. doi: 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8. Hum Mutat. 1997. PMID: 9090527

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