5 T32 HD07105-24/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

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2000	1
2001	1
2002	1
2024	0

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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.

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

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. 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

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