Manning MA - Search Results

1

Ocular measurements in fetal alcohol spectrum disorders.

Gomez DA, May PA, Tabachnick BG, Hasken JM, Lyden ER, Kalberg WO, Hoyme HE, Manning MA, Adam MP, Robinson LK, Jones KL, Buckley D, Abdul-Rahman OA. Gomez DA, et al. Among authors: manning ma. Am J Med Genet A. 2020 Oct;182(10):2243-2252. doi: 10.1002/ajmg.a.61759. Epub 2020 Jul 17. Am J Med Genet A. 2020. PMID: 32677343

2

Diagnosis and management of the adolescent boy with Klinefelter syndrome.

Manning MA, Hoyme HE. Manning MA, et al. Adolesc Med. 2002 Jun;13(2):367-74, viii. Adolesc Med. 2002. PMID: 11986043 Review.

3

Methotrexate/misoprostol embryopathy: report of four cases resulting from failed medical abortion.

Adam MP, Manning MA, Beck AE, Kwan A, Enns GM, Clericuzio C, Hoyme HE. Adam MP, et al. Among authors: manning ma. Am J Med Genet A. 2003 Nov 15;123A(1):72-8. doi: 10.1002/ajmg.a.20503. Am J Med Genet A. 2003. PMID: 14556250 Review.

4

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.

5

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

6

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.

7

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

8

Fetal alcohol spectrum disorders: a practical clinical approach to diagnosis.

Manning MA, Eugene Hoyme H. Manning MA, et al. Neurosci Biobehav Rev. 2007;31(2):230-8. doi: 10.1016/j.neubiorev.2006.06.016. Epub 2006 Sep 7. Neurosci Biobehav Rev. 2007. PMID: 16962173 Review.

9

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.

10

Sclerocornea associated with the chromosome 22q11.2 deletion syndrome.

Binenbaum G, McDonald-McGinn DM, Zackai EH, Walker BM, Coleman K, Mach AM, Adam M, Manning M, Alcorn DM, Zabel C, Anderson DR, Forbes BJ. Binenbaum G, et al. Am J Med Genet A. 2008 Apr 1;146A(7):904-9. doi: 10.1002/ajmg.a.32156. Am J Med Genet A. 2008. PMID: 18324686 Free PMC article.

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