Manning MA - Search Results

1

Acute leukemia in a patient with 15q overgrowth syndrome.

Bodle EE, Gupta R, Cherry AM, Muffly L, Manning MA. Bodle EE, et al. Among authors: manning ma. Am J Med Genet A. 2019 Jun;179(6):1025-1029. doi: 10.1002/ajmg.a.61115. Epub 2019 Mar 12. Am J Med Genet A. 2019. PMID: 30861314

2

Neu-Laxova syndrome: detailed prenatal diagnostic and post-mortem findings and literature review.

Manning MA, Cunniff CM, Colby CE, El-Sayed YY, Hoyme HE. Manning MA, et al. Am J Med Genet A. 2004 Mar 15;125A(3):240-9. doi: 10.1002/ajmg.a.20467. Am J Med Genet A. 2004. PMID: 14994231 Review.

3

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.

Manning MA, Cassidy SB, Clericuzio C, Cherry AM, Schwartz S, Hudgins L, Enns GM, Hoyme HE. Manning MA, et al. Pediatrics. 2004 Aug;114(2):451-7. doi: 10.1542/peds.114.2.451. Pediatrics. 2004. PMID: 15286229

4

A report of three patients with an interstitial deletion of chromosome 15q24.

Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, Anderson CE, Punnett HH, Thurston VC, Sweeney D, Vance GH. Cushman LJ, et al. Among authors: manning ma. Am J Med Genet A. 2005 Aug 15;137(1):65-71. doi: 10.1002/ajmg.a.30836. Am J Med Genet A. 2005. PMID: 16007617 Review.

5

Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization.

Shieh JT, Aradhya S, Novelli A, Manning MA, Cherry AM, Brumblay J, Salpietro CD, Bernardini L, Dallapiccola B, Hoyme HE. Shieh JT, et al. Among authors: manning ma. Am J Med Genet A. 2006 Jun 15;140(12):1267-73. doi: 10.1002/ajmg.a.31262. Am J Med Genet A. 2006. PMID: 16691576

6

Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.

Aradhya S, Manning MA, Splendore A, Cherry AM. Aradhya S, et al. Among authors: manning ma. Am J Med Genet A. 2007 Jul 1;143A(13):1431-41. doi: 10.1002/ajmg.a.31773. Am J Med Genet A. 2007. PMID: 17568414

7

22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay.

Cusmano-Ozog K, Manning MA, Hoyme HE. Cusmano-Ozog K, et al. Among authors: manning ma. Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):393-8. doi: 10.1002/ajmg.c.30155. Am J Med Genet C Semin Med Genet. 2007. PMID: 17926345 Review.

8

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities.

Manning M, Hudgins L; Professional Practice and Guidelines Committee. Manning M, et al. Genet Med. 2010 Nov;12(11):742-5. doi: 10.1097/GIM.0b013e3181f8baad. Genet Med. 2010. PMID: 20962661 Free PMC article.

9

Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.

Veerapandiyan A, Abdul-Rahman OA, Adam MP, Lyons MJ, Manning M, Coleman K, Kobrynski L, Taneja D, Schoch K, Zimmerman HH, Shashi V. Veerapandiyan A, et al. Am J Med Genet A. 2011 Sep;155A(9):2186-95. doi: 10.1002/ajmg.a.34226. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834039

10

Ectopia lentis as the presenting and primary feature in Marfan syndrome.

Zadeh N, Bernstein JA, Niemi AK, Dugan S, Kwan A, Liang D, Hyland JC, Hoyme HE, Hudgins L, Manning MA. Zadeh N, et al. Among authors: manning ma. Am J Med Genet A. 2011 Nov;155A(11):2661-8. doi: 10.1002/ajmg.a.34245. Epub 2011 Sep 19. Am J Med Genet A. 2011. PMID: 21932315

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