Levy B - Search Results

1

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.

Levy B, Jalal SM, Dunn TM, Warburton PE, Tonk VS, Hirschhorn K, Lockhart LH, Hughes T, Velagaleti GV. Levy B, et al. Am J Med Genet. 2002 Mar 15;108(3):198-204. doi: 10.1002/ajmg.10263. Am J Med Genet. 2002. PMID: 11891685

2

Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization.

Levy B, Gershin IF, Desnick RJ, Babu A, Gelb BD, Hirschhorn K, Cotter PD. Levy B, et al. Cytogenet Cell Genet. 1997;76(1-2):68-71. doi: 10.1159/000134518. Cytogenet Cell Genet. 1997. PMID: 9154131

3

Jumping translocations in spontaneous abortions.

Levy B, Dunn TM, Hirschhorn K, Kardon N. Levy B, et al. Cytogenet Cell Genet. 2000;88(1-2):25-9. doi: 10.1159/000015478. Cytogenet Cell Genet. 2000. PMID: 10773659

4

Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome.

Taylor Clelland CL, Levy B, McKie JM, Duncan AM, Hirschhorn K, Bancroft C. Taylor Clelland CL, et al. Among authors: levy b. Mamm Genome. 2000 Aug;11(8):675-81. doi: 10.1007/s003350010142. Mamm Genome. 2000. PMID: 10920239

5

Molecular cytogenetic analysis of uterine leiomyoma and leiomyosarcoma by comparative genomic hybridization.

Levy B, Mukherjee T, Hirschhorn K. Levy B, et al. Cancer Genet Cytogenet. 2000 Aug;121(1):1-8. doi: 10.1016/s0165-4608(00)00225-9. Cancer Genet Cytogenet. 2000. PMID: 10958933

6

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.

Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P. Levy B, et al. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

7

Clinical applications of comparative genomic hybridization.

Levy B, Dunn TM, Kaffe S, Kardon N, Hirschhorn K. Levy B, et al. Genet Med. 1998 Nov-Dec;1(1):4-12. doi: 10.1097/00125817-199811000-00004. Genet Med. 1998. PMID: 11261428 Free article.

8

Complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome.

Tadin M, Braverman E, Cianfarani S, Sobrino AJ, Levy B, Christiano AM, Warburton D. Tadin M, et al. Among authors: levy b. Am J Med Genet. 2001 Jul 22;102(1):100-4. doi: 10.1002/1096-8628(20010722)102:1<100::aid-ajmg1396>3.0.co;2-o. Am J Med Genet. 2001. PMID: 11471181

9

Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat).

Levy B, Dunn TM, Kern JH, Hirschhorn K, Kardon NB. Levy B, et al. Am J Med Genet. 2002 Mar 15;108(3):192-7. doi: 10.1002/ajmg.10261. Am J Med Genet. 2002. PMID: 11891684 Review.

10

Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.

Li S, Malafiej P, Levy B, Mahmood R, Field M, Hughes T, Lockhart LH, Wu Z, Huang M, Hirschhorn K, Velagaleti GV, Daniel A, Warburton PE. Li S, et al. Among authors: levy b. Am J Med Genet. 2002 Jul 1;110(3):258-67. doi: 10.1002/ajmg.10454. Am J Med Genet. 2002. PMID: 12116235

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