McPherson E - Search Results

1

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Fang YY, Eyre HJ, Bohlander SK, Estop A, McPherson E, Träger T, Riess O, Callen DF. Fang YY, et al. Among authors: mcpherson e. Am J Hum Genet. 1995 Nov;57(5):1137-42. Am J Hum Genet. 1995. PMID: 7485165 Free PMC article.

2

Duplication 20p identified via fluorescent in situ hybridization.

LeChien KA, McPherson E, Estop AM. LeChien KA, et al. Among authors: mcpherson e. Am J Med Genet. 1994 Apr 1;50(2):187-9. doi: 10.1002/ajmg.1320500210. Am J Med Genet. 1994. PMID: 7516625

3

Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features.

Estop AM, Mowery-Rushton PA, Cieply KM, Kochmar SJ, Sherer CR, Clemens M, Surti U, McPherson E. Estop AM, et al. Among authors: mcpherson e. J Med Genet. 1995 Oct;32(10):819-22. doi: 10.1136/jmg.32.10.819. J Med Genet. 1995. PMID: 8558564 Free PMC article.

4

Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.

Hu J, McPherson E, Surti U, Hasegawa SL, Gunawardena S, Gollin SM. Hu J, et al. Among authors: mcpherson e. Am J Med Genet. 2002 Nov 15;113(1):82-8. doi: 10.1002/ajmg.10708. Am J Med Genet. 2002. PMID: 12400070 Review.

5

Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome.

McPherson EW, Laneri G, Clemens MM, Kochmar SJ, Surti U. McPherson EW, et al. Am J Med Genet. 1997 Sep 5;71(4):430-3. doi: 10.1002/(sici)1096-8628(19970905)71:4<430::aid-ajmg11>3.0.co;2-h. Am J Med Genet. 1997. PMID: 9286450

6

Pallister-Killian and Fryns syndromes: nosology.

McPherson EW, Ketterer DM, Salsburey DJ. McPherson EW, et al. Am J Med Genet. 1993 Aug 15;47(2):241-5. doi: 10.1002/ajmg.1320470219. Am J Med Genet. 1993. PMID: 8213912

7

Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome.

Gong BT, Norwood TH, Hoehn H, McPherson E, Hall JG, Hickman R. Gong BT, et al. Among authors: mcpherson e. Hum Genet. 1976 Dec 29;35(1):117-23. doi: 10.1007/BF00295627. Hum Genet. 1976. PMID: 1002161

8

Interstitial deletion 2(p11.2p13): a rare chromosomal abnormality.

Wenger SL, McPherson EW. Wenger SL, et al. Among authors: mcpherson ew. Clin Genet. 1997 Jul;52(1):61-2. doi: 10.1111/j.1399-0004.1997.tb02516.x. Clin Genet. 1997. PMID: 9272715 Review.

9

Further delineation of the Baller-Gerold syndrome.

Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Lin AE, et al. Among authors: mcpherson e. Am J Med Genet. 1993 Feb 15;45(4):519-24. doi: 10.1002/ajmg.1320450423. Am J Med Genet. 1993. PMID: 8465861 Review.

10

Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.

Clemens M, Martsolf JT, Rogers JG, Mowery-Rushton P, Surti U, McPherson E. Clemens M, et al. Among authors: mcpherson e. Am J Med Genet. 1996 Dec 2;66(1):95-100. doi: 10.1002/(SICI)1096-8628(19961202)66:1<95::AID-AJMG26>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8957524

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