Chitayat D - Search Results

1

The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance.

Chitayat D, Sroka H, Keating S, Colby RS, Ryan G, Toi A, Blaser S, Viero S, Devisme L, Boute-Bénéjean O, Manouvrier-Hanu S, Mortier G, Loeys B, Rauch A, Bitoun P. Chitayat D, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1268-81. doi: 10.1002/ajmg.a.31788. Am J Med Genet A. 2007. PMID: 17506106

2

Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study.

Wilson RD, Chitayat D, McGillivray BC. Wilson RD, et al. Among authors: chitayat d. Am J Med Genet. 1992 Nov 15;44(5):586-90. doi: 10.1002/ajmg.1320440511. Am J Med Genet. 1992. PMID: 1481814

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

Pulmonary atresia with intact ventricular septum and hypoplastic right heart in sibs: a single gene disorder?

Chitayat D, McIntosh N, Fouron JC. Chitayat D, et al. Am J Med Genet. 1992 Feb 1;42(3):304-6. doi: 10.1002/ajmg.1320420308. Am J Med Genet. 1992. PMID: 1536166

5

Syndrome of mental retardation and distal arthrogryposis in sibs.

Chitayat D, Hodgkinson KA, Blaichman S, Chen ME, Watters GV, Khalife S, Hall JG. Chitayat D, et al. Am J Med Genet. 1991 Oct 1;41(1):49-51. doi: 10.1002/ajmg.1320410114. Am J Med Genet. 1991. PMID: 1951463

6

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

7

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG. Bamforth JS, et al. Among authors: chitayat d. Am J Med Genet. 1989 Jan;32(1):93-9. doi: 10.1002/ajmg.1320320120. Am J Med Genet. 1989. PMID: 2650550

8

Hepatocellular carcinoma in a child with familial Russell-Silver syndrome.

Chitayat D, Friedman JM, Anderson L, Dimmick JE. Chitayat D, et al. Am J Med Genet. 1988 Dec;31(4):909-14. doi: 10.1002/ajmg.1320310425. Am J Med Genet. 1988. PMID: 2853572

9

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

10

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

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