Palmer CG - Search Results

1

Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.

Sun Y, Nicholls RD, Butler MG, Saitoh S, Hainline BE, Palmer CG. Sun Y, et al. Among authors: palmer cg. Hum Mol Genet. 1996 Apr;5(4):517-24. doi: 10.1093/hmg/5.4.517. Hum Mol Genet. 1996. PMID: 8845846 Free PMC article.

2

Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.

Vance GH, Nickerson C, Sarnat L, Zhang A, Henegariu O, Morichon-Delvallez N, Butler MG, Palmer CG. Vance GH, et al. Among authors: palmer cg. Am J Med Genet. 1998 Feb 26;76(1):51-7. Am J Med Genet. 1998. PMID: 9508065 Free PMC article.

3

Marker chromosome 21 identified by microdissection and FISH.

Sun Y, Rubinstein J, Soukup S, Palmer CG. Sun Y, et al. Among authors: palmer cg. Am J Med Genet. 1995 Mar 27;56(2):151-4. doi: 10.1002/ajmg.1320560207. Am J Med Genet. 1995. PMID: 7542834

4

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Butler MG, Meaney FJ, Palmer CG. Butler MG, et al. Among authors: palmer cg. Am J Med Genet. 1986 Mar;23(3):793-809. doi: 10.1002/ajmg.1320230307. Am J Med Genet. 1986. PMID: 3953677 Free PMC article.

5

Parental origin of chromosome 15 deletion in Prader-Willi syndrome.

Butler MG, Palmer CG. Butler MG, et al. Among authors: palmer cg. Lancet. 1983 Jun 4;1(8336):1285-6. doi: 10.1016/s0140-6736(83)92745-9. Lancet. 1983. PMID: 6134086 Free PMC article. No abstract available.

6

Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findings.

Butler MG, Russell LJ, Palmer CG, Bull M, Hodes ME. Butler MG, et al. Among authors: palmer cg. Am J Med Genet. 1982 Dec;13(4):369-72. doi: 10.1002/ajmg.1320130404. Am J Med Genet. 1982. PMID: 6961772 Free PMC article.

7

Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes.

Plattner R, Heerema NA, Yurov YB, Palmer CG. Plattner R, et al. Among authors: palmer cg. Hum Genet. 1993 Mar;91(2):131-40. doi: 10.1007/BF00222713. Hum Genet. 1993. PMID: 8462972

8

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S. Leana-Cox J, et al. Among authors: palmer cg. Am J Hum Genet. 1994 May;54(5):748-56. Am J Hum Genet. 1994. PMID: 8178816 Free PMC article.

9

Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.

Wheeler PG, Weaver DD, Palmer CG. Wheeler PG, et al. Among authors: palmer cg. Am J Med Genet. 1995 Feb 13;55(4):462-5. doi: 10.1002/ajmg.1320550414. Am J Med Genet. 1995. PMID: 7762587

10

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.

Plattner R, Heerema NA, Howard-Peebles PN, Miles JH, Soukup S, Palmer CG. Plattner R, et al. Among authors: palmer cg. Hum Genet. 1993 Jul;91(6):589-98. doi: 10.1007/BF00205086. Hum Genet. 1993. PMID: 8340114

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