Chitayat D - Search Results

1

FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome.

Chun K, Siegel-Bartelt J, Chitayat D, Phillips J, Ray PN. Chun K, et al. Among authors: chitayat d. Am J Med Genet. 1998 May 18;77(3):219-24. doi: 10.1002/(sici)1096-8628(19980518)77:3<219::aid-ajmg6>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9605588

2

King syndrome: a genetically heterogenous phenotype due to congenital myopathies.

Chitayat D, Hodgkinson KA, Ginsburg O, Dimmick J, Watters GV. Chitayat D, et al. Am J Med Genet. 1992 Aug 1;43(6):954-6. doi: 10.1002/ajmg.1320430610. Am J Med Genet. 1992. PMID: 1415346 Review.

3

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

4

Acrania: a manifestation of the Adams-Oliver syndrome.

Chitayat D, Meunier C, Hodgkinson KA, Robb L, Azouz M. Chitayat D, et al. Am J Med Genet. 1992 Nov 15;44(5):562-6. doi: 10.1002/ajmg.1320440506. Am J Med Genet. 1992. PMID: 1481809

5

Autosomal recessive oral-facial-digital syndrome with resemblance to OFD types II, III, IV and VI: a new OFD syndrome?

Chitayat D, Stalker HJ, Azouz EM. Chitayat D, et al. Am J Med Genet. 1992 Nov 15;44(5):567-72. doi: 10.1002/ajmg.1320440507. Am J Med Genet. 1992. PMID: 1481810

6

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

7

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

8

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

9

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

10

Ebstein anomaly: report of a familial occurrence and prenatal diagnosis.

McIntosh N, Chitayat D, Bardanis M, Fouron JC. McIntosh N, et al. Among authors: chitayat d. Am J Med Genet. 1992 Feb 1;42(3):307-9. doi: 10.1002/ajmg.1320420309. Am J Med Genet. 1992. PMID: 1536167

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