Chudley AE - Search Results

1

Clinical genetics and the Hutterite population: a review of Mendelian disorders.

Boycott KM, Parboosingh JS, Chodirker BN, Lowry RB, McLeod DR, Morris J, Greenberg CR, Chudley AE, Bernier FP, Midgley J, Møller LB, Innes AM. Boycott KM, et al. Among authors: chudley ae. Am J Med Genet A. 2008 Apr 15;146A(8):1088-98. doi: 10.1002/ajmg.a.32245. Am J Med Genet A. 2008. PMID: 18348266 Review.

2

New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians.

Marles SL, Greenberg CR, Persaud TV, Shuckett EP, Chudley AE. Marles SL, et al. Among authors: chudley ae. Am J Med Genet. 1992 Apr 1;42(6):793-9. doi: 10.1002/ajmg.1320420609. Am J Med Genet. 1992. PMID: 1554017

3

X linked alpha thalassaemia/mental retardation (ATR-X) syndrome.

Chudley AE, Lowry RB. Chudley AE, et al. J Med Genet. 1992 May;29(5):357. doi: 10.1136/jmg.29.5.357. J Med Genet. 1992. PMID: 1583667 Free PMC article. No abstract available.

4

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

5

Paracentric inversion 11q in Canadian Hutterites.

Chodirker BN, Greenberg CR, Pabello PD, Chudley AE. Chodirker BN, et al. Among authors: chudley ae. Hum Genet. 1992 Jun;89(4):450-2. doi: 10.1007/BF00194321. Hum Genet. 1992. PMID: 1618494

6

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

7

Intrauterine growth retardation and minor anomalies in 47,XXX children.

Chudley AE, Stoeber GP, Greenberg CR. Chudley AE, et al. Birth Defects Orig Artic Ser. 1990;26(4):267-72. Birth Defects Orig Artic Ser. 1990. PMID: 2090325 No abstract available.

8

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

9

Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.

Chudley AE, Lowry RB, Hoar DI. Chudley AE, et al. Am J Med Genet. 1988 Dec;31(4):741-51. doi: 10.1002/ajmg.1320310404. Am J Med Genet. 1988. PMID: 3239563

10

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

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