An undifferentiated pediatrician von Kelly, Thaddeus E.

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

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

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836 LD-B DOSE EFFECT IN TETRASOMY 12p PSEUDOMOSAICISM von Kelly, Thaddeus E, Bruns, David E, Mifflin, Theodore E, Atkln, Joan F

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The mucopolysaccharidoses and mucolipidoses von Kelly, T E

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Clinical genetics on the road: Be Oslerian, young man von Kelly, Thaddeus E.

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Teratogenicity of anticonvulsant drugs. III: Radiographic hand analysis of children exposed in utero to diphenylhydantoin von 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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Clinical genetics on the road: In family studies go after the oldest living relatives von Kelly, Thaddeus E., Opitz, John M.

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Gonadal dysgenesis with45,XO/46,XX mosaicism demonstrated only in a streak gonad von Goldstein, David E., Kelly, Thaddeus E., Johanson, Ann J., Blizzard, Robert M.

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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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Reply to the letter to the editor by Miller-"bone loading" von Kelly, Thaddeus E.

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

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Trisomy 9p with an isochromosome of 9p: Greg smith, Alice McCaa, and Thaddeus E. Kelly Hum. Genet. 42, 93?97 (1978) von Biederman, Brian

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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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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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