Basel D - Search Results

1

Bacteremia in Patients with Heterotaxy: A Review and Implications for Management.

Loomba RS, Geddes GC, Basel D, Benson DW, Leuthner SR, Hehir DA, Ghanayem N, Shillingford AJ. Loomba RS, et al. Among authors: basel d. Congenit Heart Dis. 2016 Dec;11(6):537-547. doi: 10.1111/chd.12395. Epub 2016 Jul 18. Congenit Heart Dis. 2016. PMID: 27425254 Review.

2

Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease.

Geddes GC, Basel D, Frommelt P, Kinney A, Earing M. Geddes GC, et al. Among authors: basel d. Pediatr Cardiol. 2017 Oct;38(7):1465-1470. doi: 10.1007/s00246-017-1685-7. Epub 2017 Jul 19. Pediatr Cardiol. 2017. PMID: 28725922 Free PMC article.

3

Inheritance of a Balanced t(12;20)(q24.33;p12.2) and Unbalanced der(13)t(7;13)(p21.3;q33.2) from a Maternally Derived Double Balanced Translocation Carrier.

Peterson JF, Geddes GC, Basel DG, Schippman D, Grignon JW Jr, vanTuinen P, Kappes UP. Peterson JF, et al. Among authors: basel dg. J Pediatr Genet. 2018 Mar;7(1):35-39. doi: 10.1055/s-0037-1605592. Epub 2017 Aug 14. J Pediatr Genet. 2018. PMID: 29441220 Free PMC article.

4

A review of next-generation genetic testing for the dermatologist.

Kwon EK, Basel D, Siegel D, Martin KL. Kwon EK, et al. Among authors: basel d. Pediatr Dermatol. 2013 Jul-Aug;30(4):401-8. doi: 10.1111/pde.12062. Epub 2012 Dec 28. Pediatr Dermatol. 2013. PMID: 23278715 Review.

5

Mitochondrial DNA Depletion Syndromes.

Basel D. Basel D. Clin Perinatol. 2020 Mar;47(1):123-141. doi: 10.1016/j.clp.2019.10.008. Epub 2019 Oct 31. Clin Perinatol. 2020. PMID: 32000920 Review.

6

Adaptive behavior in young children with neurofibromatosis type 1.

Klein-Tasman BP, Colon AM, Brei N, van der Fluit F, Casnar CL, Janke KM, Basel D, Siegel DH, Walker JA. Klein-Tasman BP, et al. Among authors: basel d. Int J Pediatr. 2013;2013:690432. doi: 10.1155/2013/690432. Epub 2013 Nov 19. Int J Pediatr. 2013. PMID: 24348581 Free PMC article.

7

Alveolar capillary dysplasia with multiple congenital anomalies and bronchoscopic airway abnormalities.

Bellamkonda-Athmaram V, Sulman CG, Basel DG, Southern J, Konduri GG, Basir MA. Bellamkonda-Athmaram V, et al. Among authors: basel dg. J Perinatol. 2014 Apr;34(4):326-8. doi: 10.1038/jp.2013.175. J Perinatol. 2014. PMID: 24675018

8

A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the XIST Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33).

Peterson JF, Basel DG, Bick DP, Chirempes B, Lorier RB, Zemlicka N, Grignon JW Jr, Weik L, Kappes U. Peterson JF, et al. J Pediatr Genet. 2018 Mar;7(1):23-28. doi: 10.1055/s-0037-1604448. Epub 2017 Jul 26. J Pediatr Genet. 2018. PMID: 29441218 Free PMC article.

9

Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence.

Brar R, Basel DG, Bick DP, Weik L, vanTuinen P, Peterson JF. Brar R, et al. J Assoc Genet Technol. 2017;43(2):56-58. J Assoc Genet Technol. 2017. PMID: 28511170

10

Ending a Diagnostic Odyssey: Family Education, Counseling, and Response to Eventual Diagnosis.

Basel D, McCarrier J. Basel D, et al. Pediatr Clin North Am. 2017 Feb;64(1):265-272. doi: 10.1016/j.pcl.2016.08.017. Pediatr Clin North Am. 2017. PMID: 27894449 Review.

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