Levy B - Search Results

1

Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling.

Jobanputra V, Ash E, Anyane-Yeboa K, Warburton D, Levy B. Jobanputra V, et al. Among authors: levy b. Am J Med Genet A. 2009 Jun;149A(6):1310-4. doi: 10.1002/ajmg.a.32680. Am J Med Genet A. 2009. PMID: 19449399 No abstract available.

2

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

3

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.

4

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

5

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

6

Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation.

Shanske AL, Edelmann L, Kardon NB, Gosset P, Levy B. Shanske AL, et al. Among authors: levy b. Am J Med Genet A. 2004 Nov 15;131(1):29-35. doi: 10.1002/ajmg.a.30311. Am J Med Genet A. 2004. PMID: 15368480 Review.

7

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.

Kulharya AS, Flannery DB, Norris K, Lovell C, Levy B, Velagaleti GV. Kulharya AS, et al. Among authors: levy b. Am J Med Genet A. 2008 Sep 1;146A(17):2234-41. doi: 10.1002/ajmg.a.32397. Am J Med Genet A. 2008. PMID: 18666229

8

Preparation and culture of products of conception and other solid tissues for chromosome analysis.

Levy B, Jobanputra V, Warburton D. Levy B, et al. Curr Protoc Hum Genet. 2009 Jan;Chapter 8:Unit 8.5. doi: 10.1002/0471142905.hg0805s60. Curr Protoc Hum Genet. 2009. PMID: 19170032

9

Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA.

Shanske AL, Leonard J, Nahum O, Coppock DL, Levy B. Shanske AL, et al. Among authors: levy b. Am J Med Genet A. 2010 Dec;152A(12):3185-8. doi: 10.1002/ajmg.a.33431. Am J Med Genet A. 2010. PMID: 21108406 No abstract available.

10

The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature.

Torgyekes E, Shanske AL, Anyane-Yeboa K, Nahum O, Pirzadeh S, Blumfield E, Jobanputra V, Warburton D, Levy B. Torgyekes E, et al. Among authors: levy b. Am J Med Genet A. 2011 Aug;155A(8):1884-96. doi: 10.1002/ajmg.a.34090. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744488 Review.

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