Magenis RE - Search Results

1

Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations.

Warden CR, Pillers DA, Rice MJ, Wildes J, Livingston JS, Clark BA, Gilhooly JT, Magenis RE. Warden CR, et al. Among authors: magenis re. Am J Med Genet. 2001 Jun 15;101(2):100-5. doi: 10.1002/ajmg.1337. Am J Med Genet. 2001. PMID: 11391651

2

Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm.

Boyd LJ, Livingston JS, Brown MG, Lawce HJ, Gilhooly JT, Wildin RS, Linck LM, Magenis RE, Pillers DA. Boyd LJ, et al. Among authors: magenis re. Am J Med Genet A. 2005 Nov 1;138(4):355-60. doi: 10.1002/ajmg.a.30895. Am J Med Genet A. 2005. PMID: 16177985

3

Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.

White DM, Pillers DA, Reiss JA, Brown MG, Magenis RE. White DM, et al. Among authors: magenis re. Am J Med Genet. 1995 Jul 17;57(4):588-97. doi: 10.1002/ajmg.1320570415. Am J Med Genet. 1995. PMID: 7573135

4

Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.

Nickel RE, Pillers DA, Merkens M, Magenis RE, Driscoll DA, Emanuel BS, Zonana J. Nickel RE, et al. Among authors: magenis re. Am J Med Genet. 1994 Oct 1;52(4):445-9. doi: 10.1002/ajmg.1320520410. Am J Med Genet. 1994. PMID: 7747757

5

Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.

Pillers DA, Weleber RG, Powell BR, Hanna CE, Magenis RE, Buist NR. Pillers DA, et al. Among authors: magenis re. Am J Med Genet. 1990 May;36(1):23-8. doi: 10.1002/ajmg.1320360106. Am J Med Genet. 1990. PMID: 2159212

6

Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region.

Nickel RE, Pillers DA, Merkens M, Magenis RE, Driscoll DA, Emanuel BS, Zonana J. Nickel RE, et al. Among authors: magenis re. Eur J Pediatr Surg. 1993 Dec;3 Suppl 1:27-8. Eur J Pediatr Surg. 1993. PMID: 8130147 No abstract available.

7

Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness.

Weleber RG, Pillers DA, Powell BR, Hanna CE, Magenis RE, Buist NR. Weleber RG, et al. Among authors: magenis re. Arch Ophthalmol. 1989 Aug;107(8):1170-9. doi: 10.1001/archopht.1989.01070020236032. Arch Ophthalmol. 1989. PMID: 2667510 Review.

8

Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.

Toth-Fejel S, Magenis RE, Leff S, Brown MG, Comegys B, Lawce H, Berry T, Kesner D, Webb MJ, Olson S. Toth-Fejel S, et al. Among authors: magenis re. Am J Med Genet. 1995 Feb 13;55(4):444-52. doi: 10.1002/ajmg.1320550411. Am J Med Genet. 1995. PMID: 7762584

9

Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.

McMilin KD, Reiss JA, Brown MG, Black MH, Buckmaster DA, Durum CT, Gunter KA, Lawce HJ, Berry TL, Lamb OA, Olson CL, Weeks FF, Yoshitomi MJ, Jacky PB, Olson SB, Magenis RE. McMilin KD, et al. Among authors: magenis re. Am J Med Genet. 1998 Jun 16;78(1):36-43. Am J Med Genet. 1998. PMID: 9637421

10

Pregnancy loss in a small chorionic villus sampling series.

Clark BA, Bissonnette JM, Olson SB, Magenis RE. Clark BA, et al. Among authors: magenis re. Am J Obstet Gynecol. 1989 Aug;161(2):301-2. doi: 10.1016/0002-9378(89)90503-6. Am J Obstet Gynecol. 1989. PMID: 2764048

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