Chitayat D - Search Results

1

Prenatal detection of microtia by MRI in a fetus with trisomy 22.

Milic A, Blaser S, Robinson A, Viero S, Halliday W, Winsor E, Toi A, Thomas M, Chitayat D. Milic A, et al. Among authors: chitayat d. Pediatr Radiol. 2006 Jul;36(7):706-10. doi: 10.1007/s00247-006-0155-9. Epub 2006 Apr 25. Pediatr Radiol. 2006. PMID: 16770674

2

Familial Dandy-Walker malformation associated with macrocephaly, facial anomalies, developmental delay, and brain stem dysgenesis: prenatal diagnosis and postnatal outcome in brothers. A new syndrome?

Chitayat D, Moore L, Del Bigio MR, MacGregor D, Ben-Zeev B, Hodgkinson K, Deck J, Stothers T, Ritchie S, Toi A. Chitayat D, et al. Am J Med Genet. 1994 Oct 1;52(4):406-15. doi: 10.1002/ajmg.1320520404. Am J Med Genet. 1994. PMID: 7538262

3

Prenatal diagnosis of retinal nonattachment in the Walker-Warburg syndrome.

Chitayat D, Toi A, Babul R, Levin A, Michaud J, Summers A, Rutka J, Blaser S, Becker LE. Chitayat D, et al. Am J Med Genet. 1995 May 8;56(4):351-8. doi: 10.1002/ajmg.1320560403. Am J Med Genet. 1995. PMID: 7604843

4

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.

5

Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.

Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL. Kobrynski L, et al. Among authors: chitayat d. Am J Med Genet. 1993 Apr 1;46(1):68-71. doi: 10.1002/ajmg.1320460111. Am J Med Genet. 1993. PMID: 8494034 Review.

6

The prognostic factors in the prenatal diagnosis of the echogenic fetal lung.

Barret J, Chitayat D, Sermer M, Amankwah K, Morrow R, Toi A, Ryan G. Barret J, et al. Among authors: chitayat d. Prenat Diagn. 1995 Sep;15(9):849-53. doi: 10.1002/pd.1970150910. Prenat Diagn. 1995. PMID: 8559756

7

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.

8

Abnormalities of the intra-abdominal fetal umbilical vein: reports of four cases and a review of the literature.

Moore L, Toi A, Chitayat D. Moore L, et al. Among authors: chitayat d. Ultrasound Obstet Gynecol. 1996 Jan;7(1):21-5. doi: 10.1046/j.1469-0705.1996.07010021.x. Ultrasound Obstet Gynecol. 1996. PMID: 8932627 Free article. Review.

9

Limb defects in homozygous alpha-thalassemia: report of three cases.

Chitayat D, Silver MM, O'Brien K, Wyatt P, Waye JS, Chiu DH, Babul R, Thomas M. Chitayat D, et al. Am J Med Genet. 1997 Jan 20;68(2):162-7. doi: 10.1002/(sici)1096-8628(19970120)68:2<162::aid-ajmg8>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9028451

10

Omphalocele in Miller-Dieker syndrome: expanding the phenotype.

Chitayat D, Toi A, Babul R, Blaser S, Moola S, Yarkoni D, Sermer M, Johnson JA, Vasjar J, Teshima I. Chitayat D, et al. Am J Med Genet. 1997 Mar 31;69(3):293-8. doi: 10.1002/(sici)1096-8628(19970331)69:3<293::aid-ajmg15>3.0.co;2-m. Am J Med Genet. 1997. PMID: 9096760

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