Chitayat D - Search Results

1

Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15.

Smith AC, Shuman C, Chitayat D, Steele L, Ray PN, Bourgeois J, Weksberg R. Smith AC, et al. Among authors: chitayat d. Am J Med Genet A. 2007 Dec 15;143A(24):3010-5. doi: 10.1002/ajmg.a.32030. Am J Med Genet A. 2007. PMID: 18000906

2

Hypomelanosis of Ito--a nonspecific marker of somatic mosaicism: report of case with trisomy 18 mosaicism.

Chitayat D, Friedman JM, Johnston MM. Chitayat D, et al. Am J Med Genet. 1990 Mar;35(3):422-4. doi: 10.1002/ajmg.1320350320. Am J Med Genet. 1990. PMID: 2309792

3

Neuroblastoma in a child with Wiedemann-Beckwith syndrome.

Chitayat D, Friedman JM, Dimmick JE. Chitayat D, et al. Am J Med Genet. 1990 Mar;35(3):433-6. doi: 10.1002/ajmg.1320350322. Am J Med Genet. 1990. PMID: 2309794

4

Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome.

Chitayat D, Rothchild A, Ling E, Friedman JM, Couch RM, Yong SL, Baldwin VJ, Hall JG. Chitayat D, et al. Am J Med Genet. 1990 Aug;36(4):434-9. doi: 10.1002/ajmg.1320360412. Am J Med Genet. 1990. PMID: 2389800

5

Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.

Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H. Chitayat D, et al. Am J Med Genet. 1995 Jan 16;55(2):147-54. doi: 10.1002/ajmg.1320550203. Am J Med Genet. 1995. PMID: 7717413 Review.

6

Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.

Chitayat D, Hodgkinson K, Luke A, Winsor E, Rose T, Kalousek D. Chitayat D, et al. Am J Med Genet. 1995 Apr 10;56(3):247-51. doi: 10.1002/ajmg.1320560302. Am J Med Genet. 1995. PMID: 7778583 Review.

7

Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia.

Bernard LE, Chitayat D, Weksberg R, Van Allen MI, Langlois S. Bernard LE, et al. Among authors: chitayat d. J Med Genet. 1996 May;33(5):432-4. doi: 10.1136/jmg.33.5.432. J Med Genet. 1996. PMID: 8733060 Free PMC article.

8

Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].

Chitayat D, Babul R, Silver MM, Jay V, Teshima IE, Babyn P, Becker LE. Chitayat D, et al. Am J Med Genet. 1996 Jan 2;61(1):45-8. doi: 10.1002/(SICI)1096-8628(19960102)61:1<45::AID-AJMG9>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8741917 Review.

9

Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review.

Markovic VD, Chitayat DA, Ritchie SM, Chodakowski BA, Hutton EM. Markovic VD, et al. Among authors: chitayat da. Am J Med Genet. 1996 Feb 2;61(4):363-70. doi: 10.1002/(SICI)1096-8628(19960202)61:4<363::AID-AJMG11>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8834049 Review.

10

Tissue-specific methylation differences and cognitive function in fragile X premutation females.

Allingham-Hawkins DJ, Brown CA, Babul R, Chitayat D, Krekewich K, Humphries T, Ray PN, Teshima IE. Allingham-Hawkins DJ, et al. Among authors: chitayat d. Am J Med Genet. 1996 Aug 9;64(2):329-33. doi: 10.1002/(SICI)1096-8628(19960809)64:2<329::AID-AJMG19>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8844075

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