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Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
Conway RL, Pressman BD, Dobyns WB, Danielpour M, Lee J, Sanchez-Lara PA, Butler MG, Zackai E, Campbell L, Saitta SC, Clericuzio CL, Milunsky JM, Hoyme HE, Shieh J, Moeschler JB, Crandall B, Lauzon JL, Viskochil DH, Harding B, Graham JM Jr. Conway RL, et al. Among authors: campbell l. Am J Med Genet A. 2007 Dec 15;143A(24):2981-3008. doi: 10.1002/ajmg.a.32040. Am J Med Genet A. 2007. PMID: 18000912 Free PMC article.
Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome.
Conlin LK, Kaur M, Izumi K, Campbell L, Wilkens A, Clark D, Deardorff MA, Zackai EH, Pallister P, Hakonarson H, Spinner NB, Krantz ID. Conlin LK, et al. Among authors: campbell l. Am J Med Genet A. 2012 Dec;158A(12):3046-53. doi: 10.1002/ajmg.a.35726. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169773
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, McDonald M, Campbell L, Ming JE, Zackai EH, Bejjani BA, Shaffer LG. Ballif BC, et al. Among authors: campbell l. Mol Cytogenet. 2008 Apr 28;1:8. doi: 10.1186/1755-8166-1-8. Mol Cytogenet. 2008. PMID: 18471269 Free PMC article.
The LTAR Cropland Common Experiment at the Kellogg Biological Station.
Robertson GP, Wilke B, Ulbrich T, Haddad NM, Hamilton SK, Baas DG, Basso B, Blesh J, Boring TJ, Campbell L, Cassida KA, Charles C, Chen J, Doll JE, Guo T, Kravchenko AN, Landis DA, Marquart-Pyatt ST, Singh MP, Sprunger CD, Stegink J. Robertson GP, et al. Among authors: campbell l. J Environ Qual. 2024 Oct 16. doi: 10.1002/jeq2.20638. Online ahead of print. J Environ Qual. 2024. PMID: 39414563
2,513 results