Chudley AE - Search Results

1

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability.

Tyson C, Dawson AJ, Bal S, Tomiuk M, Anderson T, Tucker D, Riordan D, Chudoba I, Morash B, Mhanni A, Chudley AE, McGillivray B, Parslow M, Rappold G, Roeth R, Fawcett C, Qiao Y, Harvard C, Rajcan-Separovic E. Tyson C, et al. Among authors: chudley ae. Am J Med Genet A. 2009 Mar;149A(3):490-5. doi: 10.1002/ajmg.a.32535. Am J Med Genet A. 2009. PMID: 19213034

2

Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons.

Kirkilionis AJ, Chudley AE, Greenberg CR, Yan DL, McGillivray B, Hamerton JL. Kirkilionis AJ, et al. Among authors: chudley ae. Am J Med Genet. 1992 Jun 1;43(3):588-91. doi: 10.1002/ajmg.1320430316. Am J Med Genet. 1992. PMID: 1605253

3

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.

Gregory CA, Kirkilionis AJ, Greenberg CR, Chudley AE, Hamerton JL. Gregory CA, et al. Among authors: chudley ae. Am J Med Genet. 1990 Apr;35(4):536-45. doi: 10.1002/ajmg.1320350420. Am J Med Genet. 1990. PMID: 1970703

4

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: chudley ae. Am J Med Genet. 1988 Sep;31(1):145-51. doi: 10.1002/ajmg.1320310117. Am J Med Genet. 1988. PMID: 2464927

5

Interstitial deletion of the long arm of chromosome 4.

Chudley AE, Verna MR, Ray M, Riordan D. Chudley AE, et al. 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.

6

Fragile 19p13 in a family with mental illness.

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

7

Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spots.

Dawson AJ, Chodirker BN, Chudley AE. Dawson AJ, et al. Among authors: chudley ae. Biochem Mol Med. 1995 Oct;56(1):63-9. doi: 10.1006/bmme.1995.1057. Biochem Mol Med. 1995. PMID: 8593539

8

Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

Dawson AJ, Mears AJ, Chudley AE, Bech-Hansen T, McDermid H. Dawson AJ, et al. Among authors: chudley ae. J Med Genet. 1996 Nov;33(11):952-6. doi: 10.1136/jmg.33.11.952. J Med Genet. 1996. PMID: 8950677 Free PMC article.

9

Proximal interstitial 6q deletion: a recognizable syndrome.

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

10

Familial transmission of a small supernumerary marker chromosome 8 identified by FISH: an update.

Rothenmund H, Chudley AE, Dawson AJ. Rothenmund H, et al. Among authors: chudley ae. Am J Med Genet. 1997 Oct 31;72(3):339-42. doi: 10.1002/(sici)1096-8628(19971031)72:3<339::aid-ajmg17>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9332666 Review.

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