Chitayat D - Search Results

1

Middle and inner ear malformations in mutation-proven branchio-oculo-facial (BOF) syndrome: case series and review of the literature.

Carter MT, Blaser S, Papsin B, Meschino W, Reardon W, Klatt R, Babul-Hirji R, Milunsky J, Chitayat D. Carter MT, et al. Among authors: chitayat d. Am J Med Genet A. 2012 Aug;158A(8):1977-81. doi: 10.1002/ajmg.a.35436. Epub 2012 Jun 18. Am J Med Genet A. 2012. PMID: 22711382 Review.

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

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

4

Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?

Chitayat D, McGillivray BC, Rothstein R, Flodmark O, Priddy RW, Ebelt VJ, Lirenman DS, Hall JG. Chitayat D, et al. Am J Med Genet. 1990 Mar;35(3):406-14. doi: 10.1002/ajmg.1320350318. Am J Med Genet. 1990. PMID: 2309790

5

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

6

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.

7

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

8

Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesis.

Quercia N, Chitayat D, Babul-Hirji R, New MI, Daneman D. Quercia N, et al. Among authors: chitayat d. Prenat Diagn. 1998 Jan;18(1):83-5. doi: 10.1002/(sici)1097-0223(199801)18:1<83::aid-pd219>3.0.co;2-u. Prenat Diagn. 1998. PMID: 9483646

9

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

10

Fetal bilateral subdural haemorrhages. Prenatal diagnosis and spontaneous resolution by time of delivery.

Barozzino T, Sgro M, Toi A, Akouri H, Wilson S, Yeo E, Blaser S, Chitayat D. Barozzino T, et al. Among authors: chitayat d. Prenat Diagn. 1998 May;18(5):496-503. Prenat Diagn. 1998. PMID: 9621385

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