Riordan D - Search Results

1

Functional mosaic trisomy of 1q12-->1q21 resulting from X-autosome insertion translocation with random inactivation.

Vust A, Riordan D, Wickstrom D, Chudley AE, Dawson AJ. Vust A, et al. Among authors: riordan d. Clin Genet. 1998 Jul;54(1):70-3. doi: 10.1111/j.1399-0004.1998.tb03697.x. Clin Genet. 1998. PMID: 9727744

2

Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.

Chodirker BN, Ray M, McAlpine PJ, Riordan D, Vust A, Pugh D, Chudley AE. Chodirker BN, et al. Among authors: riordan d. Am J Med Genet. 1988 Sep;31(1):145-51. doi: 10.1002/ajmg.1320310117. Am J Med Genet. 1988. PMID: 2464927

3

Proximal interstitial 6q deletion: a recognizable syndrome.

Kumar R, Riordan D, Dawson AJ, Chudley AE. Kumar R, et al. Among authors: riordan d. Am J Med Genet. 1997 Aug 22;71(3):353-6. Am J Med Genet. 1997. PMID: 9268108 Review.

4

The evaluation of 15q proximal duplications by FISH.

Riordan D, Dawson AJ. Riordan D, et al. Clin Genet. 1998 Dec;54(6):517-21. doi: 10.1111/j.1399-0004.1998.tb03773.x. Clin Genet. 1998. PMID: 9894799

5

Mosaic trisomy of a small r(1) with an abnormal phenotype.

Dawson AJ, Konkin D, Riordan D, Chudley AE. Dawson AJ, et al. Among authors: riordan d. Am J Med Genet. 2001 Sep 15;103(1):32-5. doi: 10.1002/ajmg.1494. Am J Med Genet. 2001. PMID: 11562931

6

Identification of a dup(5)(p15.3) by multicolor banding.

Riordan D, Vust A, Wickstrom DE, Brown J, Chudley AE, Tomkins D, Chudoba I, Dawson AJ. Riordan D, et al. Clin Genet. 2002 Apr;61(4):277-82. doi: 10.1034/j.1399-0004.2002.610406.x. Clin Genet. 2002. PMID: 12030892

7

Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.

Dawson AJ, Putnam S, Schultz J, Riordan D, Prasad C, Greenberg CR, Chodirker BN, Mhanni AA, Chudley AE. Dawson AJ, et al. Among authors: riordan d. Clin Genet. 2002 Dec;62(6):488-94. doi: 10.1111/j.1399-0004.2002.tb02255.x. Clin Genet. 2002. PMID: 12515261

8

A unique patient with an Ullrich-Turner syndrome variant and mosaicism for a tiny r(X) and a partial proximal duplication 1q.

Dawson AJ, Wickstrom DE, Riordan D, Cardwell S, Casey R, Baldry S, Brown C. Dawson AJ, et al. Among authors: riordan d. Am J Med Genet A. 2004 Jan 30;124A(3):303-6. doi: 10.1002/ajmg.a.20302. Am J Med Genet A. 2004. PMID: 14708105

9

Fragile 19p13 in a family with mental illness.

Chodirker BN, Chudley AE, Ray M, Wickstrom DE, Riordan DL. Chodirker BN, et al. Among authors: riordan dl. Clin Genet. 1987 Jan;31(1):1-6. doi: 10.1111/j.1399-0004.1987.tb02759.x. Clin Genet. 1987. PMID: 3568428

10

Interstitial deletion of the long arm of chromosome 4.

Chudley AE, Verna MR, Ray M, Riordan D. Chudley AE, et al. Among authors: riordan d. Am J Med Genet. 1988 Nov;31(3):549-51. doi: 10.1002/ajmg.1320310309. Am J Med Genet. 1988. PMID: 3228137 No abstract available.

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