Greenberg CR - Search Results

1

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: greenberg cr. Clin Genet. 2002 Dec;62(6):488-94. doi: 10.1111/j.1399-0004.2002.tb02255.x. Clin Genet. 2002. PMID: 12515261

2

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: greenberg cr. Am J Med Genet. 1990 Apr;35(4):536-45. doi: 10.1002/ajmg.1320350420. Am J Med Genet. 1990. PMID: 1970703

3

A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort.

Elliott AM, Simard LR, Coghlan G, Chudley AE, Chodirker BN, Greenberg CR, Burch T, Ly V, Hatch GM, Zelinski T. Elliott AM, et al. Among authors: greenberg cr. J Med Genet. 2013 Dec;50(12):819-22. doi: 10.1136/jmedgenet-2013-101715. Epub 2013 Sep 24. J Med Genet. 2013. PMID: 24065355

4

Manitoba Oculotrichoanal (MOTA) syndrome: report of eight new cases.

Li C, Marles SL, Greenberg CR, Chodirker BN, van de Kamp J, Slavotinek A, Chudley AE. Li C, et al. Among authors: greenberg cr. Am J Med Genet A. 2007 Apr 15;143A(8):853-7. doi: 10.1002/ajmg.a.31446. Am J Med Genet A. 2007. PMID: 17352387

5

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: greenberg cr. Am J Med Genet. 1992 Jun 1;43(3):588-91. doi: 10.1002/ajmg.1320430316. Am J Med Genet. 1992. PMID: 1605253

6

Paracentric inversion 11q in Canadian Hutterites.

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

7

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

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

8

Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.

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

9

Low MSAFP levels and Williams syndrome.

Chodirker BN, Greenberg CR, Giddins NG, Dawson AJ, Evans JA, Chudley AE. Chodirker BN, et al. Among authors: greenberg cr. Am J Med Genet. 1997 Nov 12;72(4):448-50. doi: 10.1002/(sici)1096-8628(19971112)72:4<448::aid-ajmg14>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9375729

10

Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature.

Innes AM, Chudley AE, Reed MH, Shuckett EP, Hildes-Ripstein GE, Greenberg CR. Innes AM, et al. Among authors: greenberg cr. Am J Med Genet. 2001 Jul 22;102(1):44-7. doi: 10.1002/1096-8628(20010722)102:1<44::aid-ajmg1410>3.0.co;2-7. Am J Med Genet. 2001. PMID: 11471171 Review.

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