Back to Index
Linda M. Randolph, MD
Associate Professor of Clinical Pediatrics
CHL Mail Stop 90 Off Campus Los Angeles
+1 323 361 2178


Chmait RH, Baskin JL, Carson S, Randolph LM, Hamilton A. Treatment of alpha(0)-thalassemia (--(SEA)/--(SEA)) via serial fetal and post-natal transfusions: Can early fetal intervention improve outcomes? Hematology. 2015 May; 20(4):217-22. View in: PubMed

Sabati AA, Wong PC, Randolph L, Pruetz JD. Absent Aortic Valve Associated with Double Outlet Right Ventricle and Aortopulmonary Window: Physiologic Implications of a Rare Malformation in both the Fetus and Neonate. Congenit Heart Dis. 2014 May; 9(3):E98-E104. View in: PubMed

Shah R, Tran HC, Randolph L, Mascarenhas L, Venkatramani R. Hepatoblastoma in a 15-month-old female with trisomy 13. Am J Med Genet A. 2014 Feb; 164(2):472-5. View in: PubMed

Scheuerle AE, Picconi JL, Neidich J, Panny S, Plecher BA, Randolph LM, Trapane P, Trotter TL. The childless man. Am J Med Genet A. 2014 Feb; 164(2):561. View in: PubMed

Chen K, Chmait RH, Vanderbilt D, Wu S, Randolph L. Chimerism in monochorionic dizygotic twins: case study and review. Am J Med Genet A. 2013 Jul; 161A(7):1817-24. View in: PubMed

Dabell MP, Rosenfeld JA, Bader P, Escobar LF, El-Khechen D, Vallee SE, Dinulos MB, Curry C, Fisher J, Tervo R, Hannibal MC, Siefkas K, Wyatt PR, Hughes L, Smith R, Ellingwood S, Lacassie Y, Stroud T, Farrell SA, Sanchez-Lara PA, Randolph LM, Niyazov D, Stevens CA, Schoonveld C, Skidmore D, MacKay S, Miles JH, Moodley M, Huillet A, Neill NJ, Ellison JW, Ballif BC, Shaffer LG. Investigation of NRXN1 deletions: clinical and molecular characterization. Am J Med Genet A. 2013 Apr; 161A(4):717-31. View in: PubMed

Paquette LB, Miller D, Jackson HA, Lee T, Randolph L, Murphree AL, Panigrahy A. In utero detection of retinoblastoma with fetal magnetic resonance and ultrasound: initial experience. AJP Rep. 2012 Nov; 2(1):55-62. View in: PubMed

Patel S, Randolph LM, Benirschke K, Llanes A, Yedigarova L, Chmait RH. Prevalence of noncardiac structural anomalies in twin-twin transfusion syndrome. J Ultrasound Med. 2012 Apr; 31(4):555-60. View in: PubMed

Davidson TB, Sanchez-Lara PA, Randolph LM, Krieger MD, Wu SQ, Panigrahy A, Shimada H, Erdreich-Epstein A. Microdeletion del(22)(q12. 2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature. BMC Med Genet. 2012; 13:19. View in: PubMed

Randolph LM, Jackson HA, Wang J, Shimada H, Sanchez-Lara PA, Wong DA, Wong LJ, Boles RG. Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder. Mol Genet Metab. 2011 Feb; 102(2):149-52. View in: PubMed

Assaf SA, Randolph LM, Benirschke K, Wu S, Samadi R, Chmait RH. Discordant blood chimerism in dizygotic monochorionic laser-treated twin-twin transfusion syndrome. Obstet Gynecol. 2010 Aug; 116 Suppl 2:483-5. View in: PubMed

Kung GC, Chang PM, Sklansky MS, Randolph LM. Hypoplastic left heart syndrome in patients with Kabuki syndrome. Pediatr Cardiol. 2010 Jan; 31(1):138-41. View in: PubMed

Jackson SR, Guner YS, Woo R, Randolph LM, Ford H, Shin CE. L1CAM mutation in association with X-linked hydrocephalus and Hirschsprung's disease. Pediatr Surg Int. 2009 Sep; 25(9):823-5. View in: PubMed

Barseghyan K, Sklansky MS, Paquette LB, Randolph LM, Miller DA. Agenesis of the ductus venosus in a fetus with nonmosaic trisomy 22. Prenat Diagn. 2009 Sep; 29(9):901-2. View in: PubMed

Jackson P, Paquette L, Watiker V, Randolph L, Ramanathan R, Seri I. Intrauterine exposure to mycophenolate mofetil and multiple congenital anomalies in a newborn: possible teratogenic effect. Am J Med Genet A. 2009 Jun; 149A(6):1231-6. View in: PubMed

Powered bySC CTSI