Chitayat D - Search Results

1

Maternal SLE and brachytelephalangic chondrodysplasia punctata in a patient with unrelated de novo RAF1 and SIX2 variants.

Alkhunaizi E, Unger S, Shannon P, Nishimura G, Blaser S, Chitayat D. Alkhunaizi E, et al. Among authors: chitayat d. Am J Med Genet A. 2020 Jul;182(7):1807-1811. doi: 10.1002/ajmg.a.61621. Epub 2020 Jun 7. Am J Med Genet A. 2020. PMID: 32506814

2

Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndrome.

Chitayat D, Hodgkinson KA, Chen MF, Haber GD, Nakishima S, Sando I. Chitayat D, et al. Am J Med Genet. 1992 Aug 1;43(6):970-5. doi: 10.1002/ajmg.1320430613. Am J Med Genet. 1992. PMID: 1415348

3

Familial intestinal malrotation with midgut volvulus and facial anomalies: a disorder involving a gene controlling the normal gut rotation?

Stalker HJ, Chitayat D. Stalker HJ, et al. Among authors: chitayat d. Am J Med Genet. 1992 Sep 1;44(1):46-7. doi: 10.1002/ajmg.1320440111. Am J Med Genet. 1992. PMID: 1519649

4

Intrafamilial variability in cleidocranial dysplasia: a three generation family.

Chitayat D, Hodgkinson KA, Azouz EM. Chitayat D, et al. Am J Med Genet. 1992 Feb 1;42(3):298-303. doi: 10.1002/ajmg.1320420307. Am J Med Genet. 1992. PMID: 1536165

5

De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.

Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG. Chitayat D, et al. Am J Med Genet. 1989 Jan;32(1):36-41. doi: 10.1002/ajmg.1320320109. Am J Med Genet. 1989. PMID: 2495721

6

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

7

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.

8

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.

9

Phocomelia, oligodactyly, and acrania: the Schinzel-Phocomelia syndrome.

Chitayat D, Stalker HJ, Vekemans M, Delneste D, Azouz EM. Chitayat D, et al. Am J Med Genet. 1993 Feb 1;45(3):297-9. doi: 10.1002/ajmg.1320450304. Am J Med Genet. 1993. PMID: 8123061

10

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.

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