Li P - Search Results

1

A de novo 3.54 Mb deletion of 17q22-q23.1 associated with hydrocephalus: a case report and review of literature.

Khattab M, Xu F, Li P, Bhandari V. Khattab M, et al. Among authors: li p. Am J Med Genet A. 2011 Dec;155A(12):3082-6. doi: 10.1002/ajmg.a.34307. Epub 2011 Nov 3. Am J Med Genet A. 2011. PMID: 22052796 Review.

2

FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6.

Zhang HZ, Li P, Wang D, Huff S, Nimmakayalu M, Qumsiyeh M, Pober BR. Zhang HZ, et al. Among authors: li p. Am J Med Genet A. 2004 Jan 30;124A(3):280-7. doi: 10.1002/ajmg.a.20413. Am J Med Genet A. 2004. PMID: 14708101 Review.

3

Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.

Li P, Zhang HZ, Huff S, Nimmakayalu M, Qumsiyeh M, Yu J, Szekely A, Xu T, Pober BR. Li P, et al. Am J Med Genet A. 2006 Dec 15;140(24):2721-9. doi: 10.1002/ajmg.a.31498. Am J Med Genet A. 2006. PMID: 17103440

4

Pulmonary atresia with intact ventricular septum (PA-IVS) in monozygotic twins.

De Stefano D, Li P, Xiang B, Hui P, Zambrano E. De Stefano D, et al. Among authors: li p. Am J Med Genet A. 2008 Feb 15;146A(4):525-8. doi: 10.1002/ajmg.a.32160. Am J Med Genet A. 2008. PMID: 18203206 No abstract available.

5

Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay.

Xiang B, Li A, Valentin D, Nowak NJ, Zhao H, Li P. Xiang B, et al. Among authors: li a, li p. Am J Med Genet A. 2008 Aug 1;146A(15):1942-54. doi: 10.1002/ajmg.a.32411. Am J Med Genet A. 2008. PMID: 18627053

6

Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.

Rossi MR, DiMaio MS, Xiang B, Lu K, Kaymakcalan H, Seashore M, Mahoney MJ, Li P. Rossi MR, et al. Among authors: li p. Am J Med Genet A. 2009 Dec;149A(12):2788-94. doi: 10.1002/ajmg.a.33088. Am J Med Genet A. 2009. PMID: 19921640 Free PMC article. Review.

7

The distribution and most recent common ancestor of the 17q21 inversion in humans.

Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, Li P, Li H, Manolopoulos VG, Speed WC, Rajeevan H, Pakstis AJ, Kidd JR, Kidd KK. Donnelly MP, et al. Among authors: li h, li p. Am J Hum Genet. 2010 Feb 12;86(2):161-71. doi: 10.1016/j.ajhg.2010.01.007. Epub 2010 Jan 28. Am J Hum Genet. 2010. PMID: 20116045 Free PMC article.

8

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia.

Bajaj R, Xu F, Xiang B, Wilcox K, Diadamo AJ, Kumar R, Pietraszkiewicz A, Halene S, Li P. Bajaj R, et al. Among authors: li p. Mol Cytogenet. 2011 Jan 20;4:3. doi: 10.1186/1755-8166-4-3. Mol Cytogenet. 2011. PMID: 21251322 Free PMC article.

9

Detecting copy number status and uncovering subclonal markers in heterogeneous tumor biopsies.

Parisi F, Ariyan S, Narayan D, Bacchiocchi A, Hoyt K, Cheng E, Xu F, Li P, Halaban R, Kluger Y. Parisi F, et al. Among authors: li p. BMC Genomics. 2011 May 11;12:230. doi: 10.1186/1471-2164-12-230. BMC Genomics. 2011. PMID: 21569352 Free PMC article.

10

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization.

Li P, Pomianowski P, DiMaio MS, Florio JR, Rossi MR, Xiang B, Xu F, Yang H, Geng Q, Xie J, Mahoney MJ. Li P, et al. Am J Med Genet A. 2011 Jul;155A(7):1605-15. doi: 10.1002/ajmg.a.34043. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671377 Free PMC article.

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