Cotter PD - Search Results

1

Mild phenotype in two siblings with distal monosomy 12p13.31-->pter.

Glass IA, Trenholme A, Mildenhall L, Bailey RJ, Cotter PD. Glass IA, et al. Among authors: cotter pd. Clin Genet. 2000 May;57(5):401-5. doi: 10.1034/j.1399-0004.2000.570513.x. Clin Genet. 2000. PMID: 10852377

2

Trisomy 2q11.2-->q21.1 resulting from an unbalanced insertion in two generations.

Glass IA, Stormer P, Oei PT, Hacking E, Cotter PD. Glass IA, et al. Among authors: cotter pd. J Med Genet. 1998 Apr;35(4):319-22. doi: 10.1136/jmg.35.4.319. J Med Genet. 1998. PMID: 9598728 Free PMC article.

3

Double aneuploidy (48,XXY,+21): molecular analysis demonstrates a maternal origin.

Glass IA, Li L, Cotter PD. Glass IA, et al. Among authors: cotter pd. Eur J Med Genet. 2006 Jul-Aug;49(4):346-8. doi: 10.1016/j.ejmg.2005.12.005. Epub 2006 Jan 19. Eur J Med Genet. 2006. PMID: 16461030 No abstract available.

4

Mosaic trisomy 14 with hepatic involvement.

Iglesias A, McCurdy LD, Glass IA, Cotter PD, Illueca M, Perenyi A, Sansaricq C. Iglesias A, et al. Among authors: cotter pd. Ann Genet. 1997;40(2):104-8. Ann Genet. 1997. PMID: 9259957

5

Ring chromosome 15: characterization by array CGH.

Glass IA, Rauen KA, Chen E, Parkes J, Alberston DG, Pinkel D, Cotter PD. Glass IA, et al. Among authors: cotter pd. Hum Genet. 2006 Jan;118(5):611-7. doi: 10.1007/s00439-005-0030-z. Epub 2005 Nov 3. Hum Genet. 2006. PMID: 16267671

6

Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.

McGhee EM, Qu Y, Wohlferd MM, Goldberg JD, Norton ME, Cotter PD. McGhee EM, et al. Among authors: cotter pd. Clin Genet. 2001 Apr;59(4):274-8. doi: 10.1034/j.1399-0004.2001.590410.x. Clin Genet. 2001. PMID: 11298684

7

Monosomy 16 as the sole abnormality in myeloid malignancies.

McGhee EM, Cohen NR, Wolf JL, Ledesma CT, Cotter PD. McGhee EM, et al. Among authors: cotter pd. Cancer Genet Cytogenet. 2000 Apr 15;118(2):163-6. doi: 10.1016/s0165-4608(99)00194-6. Cancer Genet Cytogenet. 2000. PMID: 10748300 Review.

8

Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.

Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA. Klein OD, et al. Among authors: cotter pd. Clin Genet. 2004 Jun;65(6):477-82. doi: 10.1111/j.0009-9163.2004.00261.x. Clin Genet. 2004. PMID: 15151506

9

An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficits.

Doherty MJ, Glass IA, Bennett CL, Cotter PD, Watson NF, Mitchell AL, Bird TD, Farrell DF. Doherty MJ, et al. Among authors: cotter pd. Epilepsia. 2003 Dec;44(12):1529-35. doi: 10.1111/j.0013-9580.2003.61702.x. Epilepsia. 2003. PMID: 14636323 Free article.

10

Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X).

Manea SR, Gershin IF, Babu A, Willner JP, Desnick RJ, Cotter PD. Manea SR, et al. Among authors: cotter pd. Clin Genet. 1997 Dec;52(6):432-5. doi: 10.1111/j.1399-0004.1997.tb02564.x. Clin Genet. 1997. PMID: 9520254

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