Faculty

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

Publications

Phenotype of 7q11. 23 duplication: A family clinical series. Am J Med Genet A. 2017 Jan; 173(1):114-119. View in: PubMed

CHORIONIC VILLUS SAMPLING FAILS TO CONFIRM MOSAIC TRISOMY 21 FETUS AFTER POSITIVE CELL-FREE DNA. Prenat Diagn. 2016 Dec 22. View in: PubMed

Treatment of alpha(0)-thalassemia (--(SEA)/--(SEA)) via serial fetal and post-natal transfusions: Can early fetal intervention improve outcomes? Hematology. 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

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

The childless man. Am J Med Genet A. 2014 Feb; 164(2):561. View in: PubMed

Hepatoblastoma in a 15-month-old female with trisomy 13. Am J Med Genet A. 2014 Feb; 164(2):472-5. View in: PubMed

Chimerism in monochorionic dizygotic twins: case study and review. Am J Med Genet A. 2013 Jul; 161A(7):1817-24. View in: PubMed

Investigation of NRXN1 deletions: clinical and molecular characterization. Am J Med Genet A. 2013 Apr; 161A(4):717-31. View in: PubMed

In utero detection of retinoblastoma with fetal magnetic resonance and ultrasound: initial experience. AJP Rep. 2012 Nov; 2(1):55-62. View in: PubMed

Prevalence of noncardiac structural anomalies in twin-twin transfusion syndrome. J Ultrasound Med. 2012 Apr; 31(4):555-60. View in: PubMed

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

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

Discordant blood chimerism in dizygotic monochorionic laser-treated twin-twin transfusion syndrome. Obstet Gynecol. 2010 Aug; 116 Suppl 2:483-5. View in: PubMed

Hypoplastic left heart syndrome in patients with Kabuki syndrome. Pediatr Cardiol. 2010 Jan; 31(1):138-41. View in: PubMed

Agenesis of the ductus venosus in a fetus with nonmosaic trisomy 22. Prenat Diagn. 2009 Sep; 29(9):901-2. View in: PubMed

L1CAM mutation in association with X-linked hydrocephalus and Hirschsprung's disease. Pediatr Surg Int. 2009 Sep; 25(9):823-5. View in: PubMed

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

Fetal microphthalmia diagnosed by magnetic resonance imaging. Fetal Diagn Ther. 2008; 24(3):182-5. View in: PubMed

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