Lockhart LH - Search Results

1

Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.

Velagaleti GV, Bien-Willner GA, Northup JK, Lockhart LH, Hawkins JC, Jalal SM, Withers M, Lupski JR, Stankiewicz P. Velagaleti GV, et al. Among authors: lockhart lh. Am J Hum Genet. 2005 Apr;76(4):652-62. doi: 10.1086/429252. Epub 2005 Feb 22. Am J Hum Genet. 2005. PMID: 15726498 Free PMC article.

2

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.

Northup JK, Matalon R, Lockhart LH, Hawkins JC, Velagaleti GV. Northup JK, et al. Among authors: lockhart lh. Eur J Med Genet. 2011 Jul-Aug;54(4):e394-8. doi: 10.1016/j.ejmg.2011.03.011. Epub 2011 Apr 3. Eur J Med Genet. 2011. PMID: 21466863

3

De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature.

Velagaleti GV, Jalal SM, Kukolich MK, Lockhart LH, Tonk VS. Velagaleti GV, et al. Among authors: lockhart lh. Clin Genet. 2002 Mar;61(3):202-6. doi: 10.1034/j.1399-0004.2002.610306.x. Clin Genet. 2002. PMID: 12000362 Review.

4

Unusual pseudo dicentric, psu dic (1;19)(q10;q13.42), in a female with premature ovarian failure.

Northup J, Griffis K, Hawkins J, Lockhart L, Velagaleti G. Northup J, et al. Fertil Steril. 2007 Mar;87(3):697.e5-8. doi: 10.1016/j.fertnstert.2006.05.089. Epub 2006 Nov 29. Fertil Steril. 2007. PMID: 17140574 Free article.

5

Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic features.

Velagaleti GV, Jalal SM, Michaelis RC, Rowe TF, Nichols JR, Lockhart LH. Velagaleti GV, et al. Among authors: lockhart lh. Clin Dysmorphol. 2003 Jan;12(1):29-33. doi: 10.1097/00019605-200301000-00005. Clin Dysmorphol. 2003. PMID: 12514362

6

A rapid and noninvasive method for detecting tissue-limited mosaicism: detection of i(12)(p10) in buccal smear from a child with Pallister-Killian syndrome.

Velagaleti GV, Tapper JK, Rampy BA, Zhang S, Hawkins JC, Lockhart LH. Velagaleti GV, et al. Among authors: lockhart lh. Genet Test. 2003 Fall;7(3):219-23. doi: 10.1089/109065703322537232. Genet Test. 2003. PMID: 14641998

7

Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2).

Tonk VS, Jesurun CA, Morgan DL, Lockhart LH, Velagaleti GV. Tonk VS, et al. Among authors: lockhart lh. Am J Med Genet A. 2004 Jan 1;124A(1):92-5. doi: 10.1002/ajmg.a.20384. Am J Med Genet A. 2004. PMID: 14679594

8

Subtelomeric rearrangements in idiopathic mental retardation.

Velagaleti GV, Robinson SS, Rouse BM, Tonk VS, Lockhart LH. Velagaleti GV, et al. Among authors: lockhart lh. Indian J Pediatr. 2005 Aug;72(8):679-85. doi: 10.1007/BF02724077. Indian J Pediatr. 2005. PMID: 16131774

9

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

Northup JK, Gadre SA, Ge Y, Lockhart LH, Velagaleti GV. Northup JK, et al. Among authors: lockhart lh. Eur J Haematol. 2007 Feb;78(2):152-6. doi: 10.1111/j.1600-0609.2006.00798.x. Eur J Haematol. 2007. PMID: 17313561

10

Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement.

Cooke SL, Northup JK, Champaige NL, Zinser W, Edwards PA, Lockhart LH, Velagaleti GV. Cooke SL, et al. Among authors: lockhart lh. Am J Med Genet A. 2008 May 1;146A(9):1166-72. doi: 10.1002/ajmg.a.32248. Am J Med Genet A. 2008. PMID: 18302246

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

47 results

Search Page

Filters