Lehman AM - Search Results

1

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Lehman AM, McFadden D, Pugash D, Sangha K, Gibson WT, Patel MS. Lehman AM, et al. Am J Med Genet A. 2008 May 15;146A(10):1299-306. doi: 10.1002/ajmg.a.32277. Am J Med Genet A. 2008. PMID: 18398855

2

Childhood-onset hemiatrophy caused by unilateral morphea.

Lehman AM, Patel MS. Lehman AM, et al. Clin Dysmorphol. 2009 Oct;18(4):213-4. doi: 10.1097/MCD.0b013e32832a9e0c. Clin Dysmorphol. 2009. PMID: 19543082 No abstract available.

3

Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy.

Lehman AM, Eydoux P, Doherty D, Glass IA, Chitayat D, Chung BY, Langlois S, Yong SL, Lowry RB, Hildebrandt F, Trnka P. Lehman AM, et al. Am J Med Genet A. 2010 Jun;152A(6):1411-9. doi: 10.1002/ajmg.a.33416. Am J Med Genet A. 2010. PMID: 20503315 Free PMC article.

4

19p13.2 microduplication causes a Sotos syndrome-like phenotype and alters gene expression.

Lehman AM, du Souich C, Chai D, Eydoux P, Huang JL, Fok AK, Avila L, Swingland J, Delaney AD, McGillivray B, Goldowitz D, Argiropoulos B, Kobor MS, Boerkoel CF. Lehman AM, et al. Clin Genet. 2012 Jan;81(1):56-63. doi: 10.1111/j.1399-0004.2010.01615.x. Epub 2011 Jan 19. Clin Genet. 2012. PMID: 21204797

5

Fetal progeria: prenatal sonographic findings in petty syndrome.

Pugash D, Schrader KA, Dunham CP, Popescu OE, Sargent MA, Lehman AM, Yong SL, Clarke LA. Pugash D, et al. Among authors: lehman am. J Ultrasound Med. 2013 May;32(5):881-3. doi: 10.7863/ultra.32.5.881. J Ultrasound Med. 2013. PMID: 23620331 No abstract available.

6

Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia.

Pugash D, Lehman AM, Langlois S. Pugash D, et al. Among authors: lehman am. Ultrasound Obstet Gynecol. 2014 Sep;44(3):365-8. doi: 10.1002/uog.13359. Ultrasound Obstet Gynecol. 2014. PMID: 24616001 Free article.

7

Additional post-natal diagnoses following antenatal diagnosis of isolated cleft lip +/− palate.

Burnell L, Verchere C, Pugash D, Loock C, Robertson S, Lehman A. Burnell L, et al. Arch Dis Child Fetal Neonatal Ed. 2014 Jul;99(4):F286-90. doi: 10.1136/archdischild-2013-305390. Epub 2014 Mar 13. Arch Dis Child Fetal Neonatal Ed. 2014. PMID: 24625434

8

Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain.

Lehman AM, Cowan JR, McFadden DE, Patel MS. Lehman AM, et al. Am J Med Genet A. 2014 Jul;164A(7):1860-2. doi: 10.1002/ajmg.a.36529. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700809 No abstract available.

9

Diffuse angiopathy in Adams-Oliver syndrome associated with truncating DOCK6 mutations.

Lehman A, Stittrich AB, Glusman G, Zong Z, Li H, Eydoux P, Senger C, Lyons C, Roach JC, Patel M. Lehman A, et al. Am J Med Genet A. 2014 Oct;164A(10):2656-62. doi: 10.1002/ajmg.a.36685. Epub 2014 Aug 4. Am J Med Genet A. 2014. PMID: 25091416 Free PMC article.

10

Mutations in NOTCH1 cause Adams-Oliver syndrome.

Stittrich AB, Lehman A, Bodian DL, Ashworth J, Zong Z, Li H, Lam P, Khromykh A, Iyer RK, Vockley JG, Baveja R, Silva ES, Dixon J, Leon EL, Solomon BD, Glusman G, Niederhuber JE, Roach JC, Patel MS. Stittrich AB, et al. Am J Hum Genet. 2014 Sep 4;95(3):275-84. doi: 10.1016/j.ajhg.2014.07.011. Epub 2014 Aug 14. Am J Hum Genet. 2014. PMID: 25132448 Free PMC article.

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