Chitayat D - Search Results

1

Severe classical congenital muscular dystrophy and merosin expression.

Vajsar J, Chitayat D, Becker LE, Ho M, Ben-Zeev B, Jay V. Vajsar J, et al. Among authors: chitayat d. Clin Genet. 1998 Sep;54(3):193-8. doi: 10.1111/j.1399-0004.1998.tb04283.x. Clin Genet. 1998. PMID: 9788720

2

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

3

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

4

Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].

Chitayat D, Babul R, Silver MM, Jay V, Teshima IE, Babyn P, Becker LE. Chitayat D, et al. Am J Med Genet. 1996 Jan 2;61(1):45-8. doi: 10.1002/(SICI)1096-8628(19960102)61:1<45::AID-AJMG9>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8741917 Review.

5

Gonadoblastoid testicular dysplasia in Walker-Warburg syndrome.

Hung NA, Silver MM, Chitayat D, Provias J, Toi A, Jay V, Becker LE. Hung NA, et al. Among authors: chitayat d. Pediatr Dev Pathol. 1998 Sep-Oct;1(5):393-404. doi: 10.1007/s100249900054. Pediatr Dev Pathol. 1998. PMID: 9688764

6

Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.

Harrison KJ, Teshima IE, Silver MM, Jay V, Unger S, Robinson WP, James A, Levin A, Chitayat D. Harrison KJ, et al. Among authors: chitayat d. Am J Med Genet. 1998 Sep 1;79(2):103-7. Am J Med Genet. 1998. PMID: 9741467

7

Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22).

Arab S, Chitayat D, Gardner HA, Winsor EJ. Arab S, et al. Among authors: chitayat d. Clin Genet. 1999 Nov;56(5):362-6. doi: 10.1034/j.1399-0004.1999.560504.x. Clin Genet. 1999. PMID: 10668926

8

Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome.

Vajsar J, Ackerley C, Chitayat D, Becker LE. Vajsar J, et al. Among authors: chitayat d. Pediatr Neurol. 2000 Feb;22(2):139-43. doi: 10.1016/s0887-8994(99)00129-0. Pediatr Neurol. 2000. PMID: 10738921

9

Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5?

Patel MS, Becker LE, Toi A, Armstrong DL, Chitayat D. Patel MS, et al. Among authors: chitayat d. Am J Med Genet A. 2006 Mar 15;140(6):594-603. doi: 10.1002/ajmg.a.31095. Am J Med Genet A. 2006. PMID: 16470708

10

A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.

Georgiou DM, Nicolaou P, Chitayat D, Koutsou P, Babul-Hirji R, Vajsar J, Murphy J, Christodoulou K. Georgiou DM, et al. Among authors: chitayat d. Can J Neurol Sci. 2006 Aug;33(3):311-6. doi: 10.1017/s0317167100005199. Can J Neurol Sci. 2006. PMID: 17001820

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

567 results

Search Page

Filters