Kardon N - Search Results

1

Clinical applications of comparative genomic hybridization.

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

2

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: kardon nb. 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.

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. Among authors: kardon nb. 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

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: kardon nb. Genet Med. 2005 Apr;7(4):251-63. doi: 10.1097/01.gim.0000160075.96707.04. Genet Med. 2005. PMID: 15834243

5

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. Among authors: kardon n. Cytogenet Cell Genet. 2000;91(1-4):165-70. doi: 10.1159/000056839. Cytogenet Cell Genet. 2000. PMID: 11173851

6

Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis.

Gelb BD, Willner JP, Dunn TM, Kardon NB, Verloes A, Poncin J, Desnick RJ. Gelb BD, et al. Among authors: kardon nb. Am J Hum Genet. 1998 Apr;62(4):848-54. doi: 10.1086/301795. Am J Hum Genet. 1998. PMID: 9529353 Free PMC article.

7

Trisomy 1 in a clinically recognized IVF pregnancy.

Dunn TM, Grunfeld L, Kardon NB. Dunn TM, et al. Among authors: kardon nb. Am J Med Genet. 2001 Mar 1;99(2):152-3. doi: 10.1002/1096-8628(2000)9999:999<00::aid-ajmg1130>3.0.co;2-p. Am J Med Genet. 2001. PMID: 11241476

8

Jumping translocations in spontaneous abortions.

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

9

Problems in prenatal diagnosis resulting from chromosomal mosaicism.

Kardon NB, Chernay PR, Hsu LY, Martin JL, Hirschhorn K. Kardon NB, et al. Clin Genet. 1972;3(2):83-9. doi: 10.1111/j.1399-0004.1972.tb01730.x. Clin Genet. 1972. PMID: 4115480 No abstract available.

10

A differential staining technique for chromosome identification and its comparison with fluorescence technique.

Chernay PR, Kardon NB, Hsu LY, Shapiro LR, Beratis NG, Kerr J, Hirschhorn K. Chernay PR, et al. Among authors: kardon nb. Clin Genet. 1972;3(5):347-56. doi: 10.1111/j.1399-0004.1972.tb01467.x. Clin Genet. 1972. PMID: 4117329 No abstract available.

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