Irons MB - Search Results

1

Fryns syndrome with Hirschsprung disease: support for possible neural crest involvement.

Alkuraya FS, Lin AE, Irons MB, Kimonis VE. Alkuraya FS, et al. Among authors: irons mb. Am J Med Genet A. 2005 Jan 15;132A(2):226-30. doi: 10.1002/ajmg.a.30423. Am J Med Genet A. 2005. PMID: 15580636 Review.

2

Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?

Alkuraya FS, Picker J, Irons MB, Kimonis VE. Alkuraya FS, et al. Among authors: irons mb. Birth Defects Res A Clin Mol Teratol. 2005 Aug;73(8):569-71. doi: 10.1002/bdra.20165. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 15965973

3

Diagnostic utility of array-based comparative genomic hybridization in a clinical setting.

Baris HN, Tan WH, Kimonis VE, Irons MB. Baris HN, et al. Among authors: irons mb. Am J Med Genet A. 2007 Nov 1;143A(21):2523-33. doi: 10.1002/ajmg.a.31988. Am J Med Genet A. 2007. PMID: 17910064

4

Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) gene.

Baris H, Bejjani BA, Tan WH, Coulter DL, Martin JA, Storm AL, Burton BK, Saitta SC, Gajecka M, Ballif BC, Irons MB, Shaffer LG, Kimonis VE. Baris H, et al. Among authors: irons mb. Am J Med Genet A. 2006 Sep 1;140A(17):1876-9. doi: 10.1002/ajmg.a.31390. Am J Med Genet A. 2006. PMID: 16892302 No abstract available.

5

Description of a case of distal 2p trisomy by array-based comparative genomic hybridization: a high resolution genome-wide investigation for chromosomal aneuploidy in a single assay.

Roberts AE, Irons MB, Kimonis VE, Mulliken JB, Morton CC, Lee C, Listewnik M. Roberts AE, et al. Among authors: irons mb. Am J Med Genet A. 2004 Oct 1;130A(2):204-7. doi: 10.1002/ajmg.a.30223. Am J Med Genet A. 2004. PMID: 15372522 Review. No abstract available.

6

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL. Shen Y, et al. Clin Chem. 2007 Dec;53(12):2051-9. doi: 10.1373/clinchem.2007.090290. Epub 2007 Sep 27. Clin Chem. 2007. PMID: 17901113

7

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.

Ching MS, Shen Y, Tan WH, Jeste SS, Morrow EM, Chen X, Mukaddes NM, Yoo SY, Hanson E, Hundley R, Austin C, Becker RE, Berry GT, Driscoll K, Engle EC, Friedman S, Gusella JF, Hisama FM, Irons MB, Lafiosca T, LeClair E, Miller DT, Neessen M, Picker JD, Rappaport L, Rooney CM, Sarco DP, Stoler JM, Walsh CA, Wolff RR, Zhang T, Nasir RH, Wu BL; Children's Hospital Boston Genotype Phenotype Study Group. Ching MS, et al. Among authors: irons mb. Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):937-47. doi: 10.1002/ajmg.b.31063. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20468056 Free PMC article.

8

22q13.3 deletion syndrome: clinical and molecular analysis using array CGH.

Dhar SU, del Gaudio D, German JR, Peters SU, Ou Z, Bader PI, Berg JS, Blazo M, Brown CW, Graham BH, Grebe TA, Lalani S, Irons M, Sparagana S, Williams M, Phillips JA 3rd, Beaudet AL, Stankiewicz P, Patel A, Cheung SW, Sahoo T. Dhar SU, et al. Am J Med Genet A. 2010 Mar;152A(3):573-81. doi: 10.1002/ajmg.a.33253. Am J Med Genet A. 2010. PMID: 20186804 Free PMC article.

9

Cholesterol in childhood: friend or foe?: Commentary on the article by Merkens et al. on page 726.

Irons MB. Irons MB. Pediatr Res. 2004 Nov;56(5):679-81. doi: 10.1203/01.PDR.0000146398.61649.74. Pediatr Res. 2004. PMID: 15496612 Review. No abstract available.

10

The genetics clinic: where does the time go?

Irons M. Irons M. Genet Med. 2008 Sep;10(9):657-8. doi: 10.1097/gim.0b013e3181853048. Genet Med. 2008. PMID: 18978676 No abstract available.

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