Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
Mundlos, S, Otto, F, Mundlos, C, Mulliken, J.B, Aylsworth, A.S, Albright, S, Lindhout, D, Cole, W.G, Henn, W, Knoll, J.H.M, Owen, M.J, Mertelsmann, R, Zabel, B.U, Olsen, B.R
Published in Cell (30.05.1997)
Published in Cell (30.05.1997)
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Journal Article
Genetic Studies of Autistic Disorder and Chromosome 7
Ashley-Koch, A., Wolpert, C.M., Menold, M.M., Zaeem, L., Basu, S., Donnelly, S.L., Ravan, S.A., Powell, C.M., Qumsiyeh, M.B., Aylsworth, A.S., Vance, J.M., Gilbert, J.R., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.
Published in Genomics (San Diego, Calif.) (01.11.1999)
Published in Genomics (San Diego, Calif.) (01.11.1999)
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Journal Article
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome
Smith, A.C., Rubin, T., Shuman, C., Estabrooks, L., Aylsworth, A.S., McDonald, M.T., Steele, L., Ray, P.N., Weksberg, R.
Published in Cytogenetic and genome research (01.03.2006)
Published in Cytogenetic and genome research (01.03.2006)
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Journal Article
Duplication 17p11.2 in two patients: clinical features and molecular cytogenetic findings
Powell, C.M., Aylsworth, A.S., Kaiser-Rogers, K.A., Rao, K.W.
Published in Genetics in medicine (01.01.1999)
Published in Genetics in medicine (01.01.1999)
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Journal Article
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene
Seizinger, B.R., Rouleau, G.A., Ozelius, L.J., Lane, A.H., Faryniarz, A.G., Chao, M.V., Huson, S., Korf, B.R., Parry, D.M., Pericak-Vance, M.A., Collins, F.S., Hobbs, W.J., Falcone, B.G., Iannazzi, J.A., Roy, J.C., St George-Hyslop, P.H., Tanzi, R.E., Bothwell, M.A., Upadhyaya, M., Harper, P., Goldstein, A.E., Hoover, D.L., Bader, J.L., Spence, M.A., Mulvihill, J.J., Aylsworth, A.S., Vance, J.M., Rossenwasser, G.O.D., Gaskell, P.C., Roses, A.D., Martuza, R.L., Breakefield, X.O., Gusella, J.F.
Published in Cell (05.06.1987)
Published in Cell (05.06.1987)
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Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia
Scott, W K, Gaskell, P C, Lennon, F, Wolpert, C M, Menold, M M, Aylsworth, A S, Warner, C, Farrell, C D, Boustany, R M, Albright, S G, Boyd, E, Kingston, H M, Cumming, W J, Vance, J M, Pericak-Vance, M A
Published in Neurogenetics (01.11.1997)
Published in Neurogenetics (01.11.1997)
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Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1)
Pericak-Vance, M.A., Yamaoka, L.H., Vance, J.M., Small, K., Rosenwasser, G.O.D., Gaskell, P.C., Hung, W.-Y., Alberts, M.J., Haynes, C.S., Speer, M.C., Gilbert, J.R., Herbstreith, M., Aylsworth, A.S., Roses, A.D.
Published in Genomics (San Diego, Calif.) (01.12.1987)
Published in Genomics (San Diego, Calif.) (01.12.1987)
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Journal Article
Preliminary phenotypic map of chromosome 4p16 based on 4p deletions
Estabrooks, L L, Rao, K W, Driscoll, D A, Crandall, B F, Dean, J C, Ikonen, E, Korf, B, Aylsworth, A S
Published in American journal of medical genetics (17.07.1995)
Published in American journal of medical genetics (17.07.1995)
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Fragile X phenotype in a patient with a large de novo deletion in Xq27-q28
Albright, S G, Lachiewicz, A M, Tarleton, J C, Rao, K W, Schwartz, C E, Richie, R, Tennison, M B, Aylsworth, A S
Published in American journal of medical genetics (15.07.1994)
Published in American journal of medical genetics (15.07.1994)
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