Chudley A - Search Results

1

Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly.

Dawson AJ, Hovanes K, Liu J, Marles S, Greenberg C, Mhanni A, Chudley A, Frosk P, Sahoo T, Schanze D, Zenker M. Dawson AJ, et al. Among authors: chudley a. Clin Dysmorphol. 2021 Apr 1;30(2):83-88. doi: 10.1097/MCD.0000000000000351. Clin Dysmorphol. 2021. PMID: 33038106

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

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

4

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

5

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

6

Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds.

Haworth JC, Booth FA, Chudley AE, deGroot GW, Dilling LA, Goodman SI, Greenberg CR, Mallory CJ, McClarty BM, Seshia SS, et al. Haworth JC, et al. Among authors: chudley ae. J Pediatr. 1991 Jan;118(1):52-8. doi: 10.1016/s0022-3476(05)81843-8. J Pediatr. 1991. PMID: 1986098

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

Another case of microcephaly, facial clefting, and preaxial polydactyly.

Marles SL, Chudley AE. Marles SL, et al. Among authors: chudley ae. J Med Genet. 1990 Sep;27(9):593-4. doi: 10.1136/jmg.27.9.593. J Med Genet. 1990. PMID: 2231655 Free PMC article.

9

Ulnar agenesis and endocardial fibroelastosis.

Marles SL, Chudley AE. Marles SL, et al. Among authors: chudley ae. Am J Med Genet. 1990 Oct;37(2):258-60. doi: 10.1002/ajmg.1320370219. Am J Med Genet. 1990. PMID: 2248295

10

Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.

Marles SL, Chodirker BN, Greenberg CR, Chudley AE. Marles SL, et al. Among authors: chudley ae. Am J Med Genet. 1995 May 8;56(4):343-50. doi: 10.1002/ajmg.1320560402. Am J Med Genet. 1995. PMID: 7604842 Review.

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