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Found 3 results

2011
Roberson EDO, Wohler ES, Hoover-Fong JE, Lisi E, Stevens EL, Thomas GH, Leonard J, Hamosh A, Pevsner J.  2011.  Genomic analysis of partial 21q monosomies with variable phenotypes.. European journal of human genetics : EJHG. 19(2):235-8. Abstract
2009
Hoover-Fong J, Savage WJ, Lisi E, Winkelstein J, Thomas GH, Hoefsloot LH, Loeb DM.  2009.  Congenital T cell deficiency in a patient with CHARGE syndrome.. The Journal of pediatrics. 154(1):140-2. Abstract
Miller ND, Nance MA, Wohler ES, Hoover-Fong JE, Lisi E, Thomas GH, Pevsner J.  2009.  Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.. American journal of medical genetics. Part A. 149A(4):669-80. Abstract

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