The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 von Ochs, Hans D, Bennett, Craig L, Christie, Jacinda, Ramsdell, Fred, Brunkow, Mary E, Ferguson, Polly J, Whitesell, Luke, Kelly, Thaddeus E, Saulsbury, Frank T, Chance, Phillip F

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An undifferentiated pediatrician von Kelly, Thaddeus E.

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Triphalangeal thumbs with brachyectrodactyly: A sporadic case von Brown, Alaina M., Romness, Mark, Dong, Danielle A., Kelly, Thaddeus E.

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Progression of cardiac disease in emery‐dreifuss muscular dystrophy von Bialer, Martin G., Mcdaniel, Nancy L., Kelly, Thaddeus E.

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Discordant Puberty in Monozygotic Twin Sisters with Neurofibromatosis Type 1 (NFl) von Kelly, Thaddeus E., Sproul, George T., Huerta, Milagros G., Rogol, Alan D.

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Extension of Phenotype Associated with Structural Mutations in Type I Collagen: Siblings with Juvenile Osteoporosis Have an α2(I)Gly436 → Arg Substitution von Dawson, Paul A., Kelly, Thaddeus E., Marini, Joan C.

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Discordant phenotypes and 45,X/46,X,idic(Y) von Kelly, T E, Franko, J B, Rogol, A, Golden, W L

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Cervical spine anomalies and tumors in Weaver syndrome von Kelly, Thaddeus E., Alford, Bennett A., Abel, Mark

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Teratogenicity of anticonvulsant drugs. I: Review of the literature von Kelly, Thaddeus E.

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Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported cases von Shashi, V, Zunich, J, Kelly, T E, Fryburg, J S

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Extension of Phenotype Associated with Structural Mutations in Type I Collagen: Siblings with Juvenile Osteoporosis have anα2(I)Gly436->Arg Substitution. † 597 von Dawson, Paul A., Kelly, Thaddeus E., Marini, Joan C.

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Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43 von KELLY, THADDEUS E, BLANTON, SUSAN, SAIF, RAMLA, SANJAD, SAMI A, SAKATI, NADIA A

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Observations Suggesting Allelism of the Achondroplasia and Hypochondroplasia Genes von McKusick, Victor A., Kelly, Thaddeus E., Dorst, John P.

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Confined placental mosaicism for trisomy 8 and intra-uterine growth retardation von Saks, Emily, McCoy, M. Cathleen, Damron, Joseph, Kelly, Thaddeus E.

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Multiple areas of intestinal atresia associated with immunodeficiency and posttransfusion graft-versus-host disease von Walker, M. Whit, Lovell, Mark A., Kelly, Thaddeus E., Golden, Wendy, Saulsbury, Frank T.

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CONGENITAL FAMILIAL CARDIAC CONDUCTION DEFECTS von GAZES, P C, CULLER, R M, TABER, E, KELLY, T E

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Gastrointestinal involvement in a woman with dyskeratosis congenita von Brown, K E, Kelly, T E, Myers, B M

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Molecular basis of hexosamininidase a deficiency and pseudodeficiency in the Berks County Pennsylvania Dutch von Mules, Emilie H., Hayflick, Susan, Dowling, Carol E., Kelly, Thaddeus E., Akerman, Beverly R., Gravel, Roy A., Thomas, George H.

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An autosomal dominant syndrome of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema von Schmitt, Edward, Gillenwater, Jay Y., Kelly, Thaddeus E., Opitz, John M.

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Identification of a mutation in the type X collagen gene (COL10A1) in a family with Schmid metaphyseal chondrodysplasia von Dharmavaram, Rita M., Elberson, Margaret A., Peng, Minzhong, Kirson, Lisa A., Kelly, Thaddeus E., Jimenez, Sergio A.

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