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Items: 1 to 50 of 136

1.

Associations between PM2.5 and risk of preterm birth among liveborn infants.

Alman BL, Stingone JA, Yazdy M, Botto LD, Desrosiers TA, Pruitt S, Herring AH, Langlois PH, Nembhard WN, Shaw GM, Olshan AF, Luben TJ; National Birth Defects Prevention Study.

Ann Epidemiol. 2019 Nov;39:46-53.e2. doi: 10.1016/j.annepidem.2019.09.008. Epub 2019 Oct 9.

PMID:
31678056
2.

Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 years.

Kurdi AM, Majeed-Saidan MA, Al Rakaf MS, AlHashem AM, Botto LD, Baaqeel HS, Ammari AN.

BMJ Open. 2019 Sep 5;9(9):e026351. doi: 10.1136/bmjopen-2018-026351.

3.

Specific birth defects in pregnancies of women with diabetes: National Birth Defects Prevention Study, 1997-2011.

Tinker SC, Gilboa SM, Moore CA, Waller DK, Simeone RM, Kim SY, Jamieson DJ, Botto LD, Reefhuis J; National Birth Defects Prevention Study.

Am J Obstet Gynecol. 2019 Aug 24. pii: S0002-9378(19)31030-0. doi: 10.1016/j.ajog.2019.08.028. [Epub ahead of print]

PMID:
31454511
4.

Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study.

Bakker MK, Bergman JEH, Krikov S, Amar E, Cocchi G, Cragan J, de Walle HEK, Gatt M, Groisman B, Liu S, Nembhard WN, Pierini A, Rissmann A, Chidambarathanu S, Sipek A Jr, Szabova E, Tagliabue G, Tucker D, Mastroiacovo P, Botto LD.

BMJ Open. 2019 Jul 2;9(7):e028139. doi: 10.1136/bmjopen-2018-028139.

5.

Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants.

Brunelli L, Jenkins SM, Gudgeon JM, Bleyl SB, Miller CE, Tvrdik T, Dames SA, Ostrander B, Daboub JAF, Zielinski BA, Zinkhan EK, Underhill HR, Wilson T, Bonkowsky JL, Yost CC, Botto LD, Jenkins J, Pysher TJ, Bayrak-Toydemir P, Mao R.

Mol Genet Genomic Med. 2019 Jul;7(7):e00796. doi: 10.1002/mgg3.796. Epub 2019 Jun 13.

6.

Public Health Approach to Improve Outcomes for Congenital Heart Disease Across the Life Span.

Jenkins KJ, Botto LD, Correa A, Foster E, Kupiec JK, Marino BS, Oster ME, Stout KK, Honein MA.

J Am Heart Assoc. 2019 Apr 16;8(8):e009450. doi: 10.1161/JAHA.118.009450. No abstract available.

7.

Join World Birth Defects Day.

Groisman B, Bermejo-Sánchez E, Romitti PA, Botto LD, Feldkamp ML, Walani SR, Mastroiacovo P.

Pediatr Res. 2019 Jul;86(1):3-4. doi: 10.1038/s41390-019-0392-x. Epub 2019 Apr 9. No abstract available.

PMID:
30965352
8.

Risk of gastroschisis with maternal genitourinary infections: the US National birth defects prevention study 1997-2011.

Feldkamp ML, Arnold KE, Krikov S, Reefhuis J, Almli LM, Moore CA, Botto LD.

BMJ Open. 2019 Mar 30;9(3):e026297. doi: 10.1136/bmjopen-2018-026297.

9.

Risk factors associated with the development of double-inlet ventricle congenital heart disease.

Paige SL, Yang W, Priest JR, Botto LD, Shaw GM, Collins RT 2nd; National Birth Defects Prevention Study.

Birth Defects Res. 2019 Jul 1;111(11):640-648. doi: 10.1002/bdr2.1501. Epub 2019 Mar 28.

PMID:
30920163
10.

Identification of fibrinogen as a natural inhibitor of MMP-2.

Sarker H, Hardy E, Haimour A, Maksymowych WP, Botto LD, Fernandez-Patron C.

Sci Rep. 2019 Mar 13;9(1):4340. doi: 10.1038/s41598-019-40983-y.

11.

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics, Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study, Hedrich UBS, Scheffer IE, Helbig I, Zamponi GW, Lerche H, Mefford HC.

Am J Hum Genet. 2019 Mar 7;104(3):562. doi: 10.1016/j.ajhg.2019.02.015. No abstract available.

12.

SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals.

Ng BG, Sosicka P, Agadi S, Almannai M, Bacino CA, Barone R, Botto LD, Burton JE, Carlston C, Chung BH, Cohen JS, Coman D, Dipple KM, Dorrani N, Dobyns WB, Elias AF, Epstein L, Gahl WA, Garozzo D, Hammer TB, Haven J, Héron D, Herzog M, Hoganson GE, Hunter JM, Jain M, Juusola J, Lakhani S, Lee H, Lee J, Lewis K, Longo N, Lourenço CM, Mak CCY, McKnight D, Mendelsohn BA, Mignot C, Mirzaa G, Mitchell W, Muhle H, Nelson SF, Olczak M, Palmer CGS, Partikian A, Patterson MC, Pierson TM, Quinonez SC, Regan BM, Ross ME, Guillen Sacoto MJ, Scaglia F, Scheffer IE, Segal D, Singhal NS, Striano P, Sturiale L, Symonds JD, Tang S, Vilain E, Willis M, Wolfe LA, Yang H, Yano S, Powis Z, Suchy SF, Rosenfeld JA, Edmondson AC, Grunewald S, Freeze HH.

Hum Mutat. 2019 Jul;40(7):908-925. doi: 10.1002/humu.23731. Epub 2019 Apr 24.

PMID:
30817854
13.

An evolutionary and developmental biology approach to gastroschisis.

Opitz JM, Feldkamp ML, Botto LD.

Birth Defects Res. 2019 Apr 1;111(6):294-311. doi: 10.1002/bdr2.1481. Epub 2019 Feb 28.

PMID:
30816021
14.

Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2.

Pekkinen M, Terhal PA, Botto LD, Henning P, Mäkitie RE, Roschger P, Jain A, Kol M, Kjellberg MA, Paschalis EP, van Gassen K, Murray M, Bayrak-Toydemir P, Magnusson MK, Jans J, Kausar M, Carey JC, Somerharju P, Lerner UH, Olkkonen VM, Klaushofer K, Holthuis JC, Mäkitie O.

JCI Insight. 2019 Apr 4;4(7). pii: 126180. doi: 10.1172/jci.insight.126180. eCollection 2019 Apr 4.

15.

Expanding the genetic and clinical spectrum of the NONO-associated X-linked intellectual disability syndrome.

Carlston CM, Bleyl SB, Andrews A, Meyers L, Brown S, Bayrak-Toydemir P, Bale JF, Botto LD.

Am J Med Genet A. 2019 May;179(5):792-796. doi: 10.1002/ajmg.a.61091. Epub 2019 Feb 17.

PMID:
30773818
16.

Application of quality indicators to data from the National Network of Congenital Anomalies of Argentina.

Groisman B, Barbero P, Mastroiacovo P, Botto LD, Bidondo MP, Liascovich R.

Birth Defects Res. 2019 Apr 1;111(6):333-340. doi: 10.1002/bdr2.1472. Epub 2019 Feb 13.

PMID:
30756506
17.

A proposal for the systematic assessment of data quality indicators in birth defects surveillance.

Groisman B, Mastroiacovo P, Barbero P, Bidondo MP, Liascovich R, Botto LD.

Birth Defects Res. 2019 Apr 1;111(6):324-332. doi: 10.1002/bdr2.1474. Epub 2019 Feb 11.

PMID:
30746866
18.

Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions.

Dugan SL, Panza E, Openshaw A, Botto LD, Camacho JA, Toydemir RM.

Am J Med Genet A. 2018 Dec;176(12):2901-2906. doi: 10.1002/ajmg.a.40664. Epub 2018 Oct 22.

PMID:
30346094
19.

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics, Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study, Hedrich UBS, Scheffer IE, Helbig I, Zamponi GW, Lerche H, Mefford HC.

Am J Hum Genet. 2018 Nov 1;103(5):666-678. doi: 10.1016/j.ajhg.2018.09.006. Epub 2018 Oct 18. Erratum in: Am J Hum Genet. 2019 Mar 7;104(3):562.

20.

Early Childhood Inpatient Costs of Critical Congenital Heart Disease.

Pinto NM, Waitzman N, Nelson R, Minich LL, Krikov S, Botto LD.

J Pediatr. 2018 Dec;203:371-379.e7. doi: 10.1016/j.jpeds.2018.07.060. Epub 2018 Sep 26.

PMID:
30268400
21.

Value of sharing and networking among birth defects surveillance programs: an ICBDSR perspective.

Bermejo-Sánchez E, Botto LD, Feldkamp ML, Groisman B, Mastroiacovo P.

J Community Genet. 2018 Oct;9(4):411-415. doi: 10.1007/s12687-018-0387-z. Epub 2018 Sep 18.

22.

Brief Report: Pediatrician Perspectives Regarding Genetic Evaluations of Children with Autism Spectrum Disorder.

Rutz A, Dent KM, Botto LD, Young PC, Carbone PS.

J Autism Dev Disord. 2019 Feb;49(2):794-808. doi: 10.1007/s10803-018-3738-z.

PMID:
30173310
23.

Intracranial Calcifications in Young Children.

Dugan SL, Botto LD, Hedlund GL, Bale JF Jr.

Semin Pediatr Neurol. 2018 Jul;26:135-139. doi: 10.1016/j.spen.2017.03.022. Epub 2017 Apr 2.

PMID:
29961505
24.

From cause to care: Triple surveillance for better outcomes in birth defects and rare diseases.

Botto LD, Mastroiacovo P.

Eur J Med Genet. 2018 Sep;61(9):551-555. doi: 10.1016/j.ejmg.2018.06.007. Epub 2018 Jun 12. Review.

PMID:
29902591
25.

Case Definitions for Conditions Identified by Newborn Screening Public Health Surveillance.

Sontag MK, Sarkar D, Comeau AM, Hassell K, Botto LD, Parad R, Rose SR, Wintergerst KA, Smith-Whitley K, Singh S, Yusuf C, Ojodu J, Copeland S, Hinton CF.

Int J Neonatal Screen. 2018;4(2):16. doi: 10.3390/ijns4020016. Epub 2018 May 9.

26.

Does Maternal Exposure to Secondhand Tobacco Smoke During Pregnancy Increase the Risk for Preterm or Small-for-Gestational Age Birth?

Hoyt AT, Canfield MA, Romitti PA, Botto LD, Anderka MT, Krikov SV, Feldkamp ML.

Matern Child Health J. 2018 Oct;22(10):1418-1429. doi: 10.1007/s10995-018-2522-1.

PMID:
29574536
27.

Triple surveillance: a proposal for an integrated strategy to support and accelerate birth defect prevention.

Botto LD, Mastroiacovo P.

Ann N Y Acad Sci. 2018 Feb;1414(1):126-136. doi: 10.1111/nyas.13600.

28.

Improving maternal folate status to prevent infant neural tube defects: working group conclusions and a framework for action.

Martinez H, Weakland AP, Bailey LB, Botto LD, De-Regil LM, Brown KH.

Ann N Y Acad Sci. 2018 Feb;1414(1):5-19. doi: 10.1111/nyas.13593.

PMID:
29532514
29.

Epidemiology and Prognosis of Congenital Diaphragmatic Hernia: A Population-Based Cohort Study in Utah.

Shanmugam H, Brunelli L, Botto LD, Krikov S, Feldkamp ML.

Birth Defects Res. 2017 Nov 1;109(18):1451-1459. doi: 10.1002/bdr2.1106. Epub 2017 Sep 19.

PMID:
28925604
30.

Etiology and clinical presentation of birth defects: population based study.

Feldkamp ML, Carey JC, Byrne JLB, Krikov S, Botto LD.

BMJ. 2017 May 30;357:j2249. doi: 10.1136/bmj.j2249.

31.

Maternal Exposure to Nitrogen Dioxide, Intake of Methyl Nutrients, and Congenital Heart Defects in Offspring.

Stingone JA, Luben TJ, Carmichael SL, Aylsworth AS, Botto LD, Correa A, Gilboa SM, Langlois PH, Nembhard WN, Richmond-Bryant J, Shaw GM, Olshan AF; National Birth Defects Prevention Study.

Am J Epidemiol. 2017 Sep 15;186(6):719-729. doi: 10.1093/aje/kwx139.

32.

Mild orotic aciduria in UMPS heterozygotes: a metabolic finding without clinical consequences.

Wortmann SB, Chen MA, Colombo R, Pontoglio A, Alhaddad B, Botto LD, Yuzyuk T, Coughlin CR, Descartes M, Grűnewald S, Maranda B, Mills PB, Pitt J, Potente C, Rodenburg R, Kluijtmans LA, Sampath S, Pai EF, Wevers RA, Tiller GE; additional individual contributors.

J Inherit Metab Dis. 2017 May;40(3):423-431. doi: 10.1007/s10545-017-0015-9. Epub 2017 Feb 15.

33.

Associations between maternal periconceptional exposure to secondhand tobacco smoke and major birth defects.

Hoyt AT, Canfield MA, Romitti PA, Botto LD, Anderka MT, Krikov SV, Tarpey MK, Feldkamp ML.

Am J Obstet Gynecol. 2016 Nov;215(5):613.e1-613.e11. doi: 10.1016/j.ajog.2016.07.022. Epub 2016 Jul 18.

PMID:
27443814
34.

Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy.

Colin E, Daniel J, Ziegler A, Wakim J, Scrivo A, Haack TB, Khiati S, Denommé AS, Amati-Bonneau P, Charif M, Procaccio V, Reynier P, Aleck KA, Botto LD, Herper CL, Kaiser CS, Nabbout R, N'Guyen S, Mora-Lorca JA, Assmann B, Christ S, Meitinger T, Strom TM, Prokisch H; FREX Consortium, Miranda-Vizuete A, Hoffmann GF, Lenaers G, Bomont P, Liebau E, Bonneau D.

Am J Hum Genet. 2016 Sep 1;99(3):695-703. doi: 10.1016/j.ajhg.2016.06.030. Epub 2016 Aug 18.

35.

Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling.

Cetinkaya A, Xiong JR, Vargel İ, Kösemehmetoğlu K, Canter Hİ, Gerdan ÖF, Longo N, Alzahrani A, Camps MP, Taskiran EZ, Laupheimer S, Botto LD, Paramalingam E, Gormez Z, Uz E, Yuksel B, Ruacan Ş, Sağıroğlu MŞ, Takahashi T, Reversade B, Akarsu NA.

Am J Hum Genet. 2016 Aug 4;99(2):299-317. doi: 10.1016/j.ajhg.2016.06.008. Epub 2016 Jul 28.

36.

Effect of dietary lysine restriction and arginine supplementation in two patients with pyridoxine-dependent epilepsy.

Yuzyuk T, Thomas A, Viau K, Liu A, De Biase I, Botto LD, Pasquali M, Longo N.

Mol Genet Metab. 2016 Jul;118(3):167-72. doi: 10.1016/j.ymgme.2016.04.015. Epub 2016 May 8.

PMID:
27324284
37.

Diagnosis, Treatment, and Clinical Outcome of Patients with Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency.

De Biase I, Viau KS, Liu A, Yuzyuk T, Botto LD, Pasquali M, Longo N.

JIMD Rep. 2017;31:63-71. doi: 10.1007/8904_2016_558. Epub 2016 Apr 28.

38.

Bayesian multinomial probit modeling of daily windows of susceptibility for maternal PM2.5 exposure and congenital heart defects.

Warren JL, Stingone JA, Herring AH, Luben TJ, Fuentes M, Aylsworth AS, Langlois PH, Botto LD, Correa A, Olshan AF; National Birth Defects Prevention Study.

Stat Med. 2016 Jul 20;35(16):2786-801. doi: 10.1002/sim.6891. Epub 2016 Feb 7.

39.

Building capacity for birth defects surveillance in Africa: Implementation of an intermediate birth defects surveillance workshop.

Flores A, Valencia D, Sekkarie A, Hillard CL, Williams J, Groisman B, Botto LD, Peña-Rosas JP, Bauwens L, Mastroiacovo P.

J Glob Health Perspect. 2015;2015. pii: 1. Epub 2015 Dec 19.

40.

Elevated body mass index and decreased diet quality among women and risk of birth defects in their offspring.

Carmichael SL, Yang W, Gilboa S, Ailes E, Correa A, Botto LD, Feldkamp ML, Shaw GM; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2016 Mar;106(3):164-71. doi: 10.1002/bdra.23471. Epub 2015 Dec 14.

41.

Clinical presentation and survival in a population-based cohort of infants with gastroschisis in Utah, 1997-2011.

Feldkamp ML, Botto LD, Byrne JLB, Krikov S, Carey JC.

Am J Med Genet A. 2016 Feb;170A(2):306-315. doi: 10.1002/ajmg.a.37437. Epub 2015 Oct 16.

PMID:
26473400
42.

Chlamydia trachomatis IgG3 seropositivity is associated with gastroschisis.

Feldkamp ML, Enioutina EY, Botto LD, Krikov S, Byrne JL, Geisler WM.

J Perinatol. 2015 Nov;35(11):930-4. doi: 10.1038/jp.2015.115. Epub 2015 Sep 17.

43.

Turner Syndrome in Girls Presenting with Coarctation of the Aorta.

Eckhauser A, South ST, Meyers L, Bleyl SB, Botto LD.

J Pediatr. 2015 Nov;167(5):1062-6. doi: 10.1016/j.jpeds.2015.08.002. Epub 2015 Aug 29.

PMID:
26323199
44.

Lower rate of selected congenital heart defects with better maternal diet quality: a population-based study.

Botto LD, Krikov S, Carmichael SL, Munger RG, Shaw GM, Feldkamp ML; National Birth Defects Prevention Study.

Arch Dis Child Fetal Neonatal Ed. 2016 Jan;101(1):F43-9. doi: 10.1136/archdischild-2014-308013. Epub 2015 Aug 24.

PMID:
26304461
45.

Evaluating cost and resource use associated with pulse oximetry screening for critical congenital heart disease: Empiric estimates and sources of variation.

Reeder MR, Kim J, Nance A, Krikov S, Feldkamp ML, Randall H, Botto LD.

Birth Defects Res A Clin Mol Teratol. 2015 Nov;103(11):962-71. doi: 10.1002/bdra.23414. Epub 2015 Jul 28.

PMID:
26215888
46.

Maternal periconceptional alcohol consumption and congenital heart defects.

Zhu Y, Romitti PA, Caspers Conway KM, Shen DH, Sun L, Browne ML, Botto LD, Lin AE, Druschel CM; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2015 Jul;103(7):617-29. doi: 10.1002/bdra.23352. Epub 2015 Jun 27.

PMID:
26118863
47.

Reflections on the etiology of structural birth defects: Established teratogens and risk factors.

Feldkamp ML, Botto LD, Carey JC.

Birth Defects Res A Clin Mol Teratol. 2015 Aug;103(8):652-5. doi: 10.1002/bdra.23392. Epub 2015 Jun 20.

PMID:
26097048
48.

Risk factors for Dandy-Walker malformation: a population-based assessment.

Reeder MR, Botto LD, Keppler-Noreuil KM, Carey JC, Byrne JL, Feldkamp ML; National Birth Defects Prevention Study.

Am J Med Genet A. 2015 Sep;167A(9):2009-16. doi: 10.1002/ajmg.a.37124. Epub 2015 May 1.

PMID:
25941000
49.

Better diet quality before pregnancy is associated with reduced risk of gastroschisis in Hispanic women.

Feldkamp ML, Krikov S, Botto LD, Shaw GM, Carmichael SL; National Birth Defects Prevention Study.

J Nutr. 2014 Nov;144(11):1781-6. doi: 10.3945/jn.114.201376. Epub 2014 Sep 24.

50.

Prevalence of variants in methylenetetrahydrofolate reductase and the severity of pulmonary vascular disease.

Day RW, Mack GK, Barker AM, Rees TQ, Jorgensen LO, Botto LD.

Pediatr Cardiol. 2015 Mar;36(3):524-30. doi: 10.1007/s00246-014-1044-x. Epub 2014 Oct 11.

PMID:
25304246

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