Chitayat D - Search Results

1

Malignant hematological disorders in children with Wolf-Hirschhorn syndrome.

Sharathkumar A, Kirby M, Freedman M, Abdelhaleem M, Chitayat D, Teshima IE, Dror Y. Sharathkumar A, et al. Among authors: chitayat d. Am J Med Genet A. 2003 Jun 1;119A(2):194-9. doi: 10.1002/ajmg.a.20080. Am J Med Genet A. 2003. PMID: 12749063

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

Interstitial tandem direct duplication of the long arm of chromosome 4 (q23-q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segment.

Halal F, Vekemans M, Chitayat D. Halal F, et al. Among authors: chitayat d. Am J Med Genet. 1991 Jun 15;39(4):418-21. doi: 10.1002/ajmg.1320390412. Am J Med Genet. 1991. PMID: 1877620

5

Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.

Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ. Chitayat D, et al. Am J Med Genet. 1990 Sep;37(1):65-70. doi: 10.1002/ajmg.1320370116. Am J Med Genet. 1990. PMID: 2240046

6

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

7

Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis.

Chitayat D, McGillivray BC, Wood S, Kalousek DK, Langlois S, Applegarth DA. Chitayat D, et al. Am J Med Genet. 1988 Nov;31(3):655-61. doi: 10.1002/ajmg.1320310321. Am J Med Genet. 1988. PMID: 3228144

8

Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing.

Hain RD, Chitayat D, Cooper R, Bandler E, Eng B, Chui DH, Waye JS, Freedman MH. Hain RD, et al. Among authors: chitayat d. Hum Mutat. 1994;3(3):239-42. doi: 10.1002/humu.1380030310. Hum Mutat. 1994. PMID: 7517266

9

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

10

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.

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