Manning MA - Search Results

1

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

2

Intracranial hemorrhage in infants and children with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome).

Morgan T, McDonald J, Anderson C, Ismail M, Miller F, Mao R, Madan A, Barnes P, Hudgins L, Manning M. Morgan T, et al. Pediatrics. 2002 Jan;109(1):E12. doi: 10.1542/peds.109.1.e12. Pediatrics. 2002. PMID: 11773580

3

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.

4

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.

5

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.

6

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

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

Use of array-based technology in the practice of medical genetics.

Manning M, Hudgins L. Manning M, et al. Genet Med. 2007 Sep;9(9):650-3. doi: 10.1097/gim.0b013e31814cec3a. Genet Med. 2007. PMID: 17873654

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

Developmental pathogenesis of short palpebral fissure length in children with fetal alcohol syndrome.

Jones KL, Hoyme HE, Robinson LK, del Campo M, Manning MA, Bakhireva LN, Prewitt LM, Chambers CD. Jones KL, et al. Among authors: manning ma. Birth Defects Res A Clin Mol Teratol. 2009 Aug;85(8):695-9. doi: 10.1002/bdra.20585. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19350654 Free PMC article.

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