Levy B - Search Results

1

Clinical and genomic characterization of 8p cytogenomic disorders.

Okur V, Hamm L, Kavus H, Mebane C, Robinson S, Levy B, Chung WK. Okur V, et al. Among authors: levy b. Genet Med. 2021 Dec;23(12):2342-2351. doi: 10.1038/s41436-021-01270-2. Epub 2021 Jul 19. Genet Med. 2021. PMID: 34282301 Free article.

2

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.

3

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

4

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.

5

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

6

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

7

Incidence and spectrum of chromosome abnormalities in spontaneous abortions: new insights from a 12-year study.

Menasha J, Levy B, Hirschhorn K, Kardon NB. Menasha J, et al. Among authors: levy b. Genet Med. 2005 Apr;7(4):251-63. doi: 10.1097/01.gim.0000160075.96707.04. Genet Med. 2005. PMID: 15834243

8

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.

9

Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis.

Levy B, Wang D, Ullner PM, Engelstad K, Yang H, Nahum O, Chung WK, De Vivo DC. Levy B, et al. Mol Genet Metab. 2010 Jun;100(2):129-35. doi: 10.1016/j.ymgme.2010.03.007. Epub 2010 Mar 17. Mol Genet Metab. 2010. PMID: 20382060

10

Glut1 deficiency: inheritance pattern determined by haploinsufficiency.

Rotstein M, Engelstad K, Yang H, Wang D, Levy B, Chung WK, De Vivo DC. Rotstein M, et al. Among authors: levy b. Ann Neurol. 2010 Dec;68(6):955-8. doi: 10.1002/ana.22088. Ann Neurol. 2010. PMID: 20687207 Free PMC article.

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