X-Linked Syndrome of Polyendocrinopathy, Immune Dysfunction, and Diarrhea Maps to Xp11.23-Xq13.3 von Bennett, Craig L., Yoshioka, Ritsuko, Kiyosawa, Hidenori, Barker, David F., Fain, Pamela R., Shigeoka, Ann O., Chance, Phillip F.

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Parental Origin–Dependent, Male Offspring–Specific Transmission-Ratio Distortion at Loci on the Human X Chromosome von Naumova, A.K., Leppert, M., Barker, D.F., Morgan, K., Sapienza, C.

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Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome von Barker, David F., Hostikka, Sirkka Liisa, Zhou, Jing, Chow, Louise T., Oliphant, Arnold R., Gerken, Steven C., Gregory, Martin C., Skolnick, Mark H., Atkin, Curtis L., Tryggvason, Karl

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Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syn... von Heath, Karen E., Campos-Barros, Angel, Toren, Amos, Rozenfeld-Granot, Galit, Carlsson, Lena E., Savige, Judy, Denison, Joyce C., Gregory, Martin C., White, James G., Barker, David F, Greinacher, Andreas, Epstein, Charles J., Glucksman, Marc J., Martignetti, John A.

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Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia von CAMBI, F, TANG, X.-M, CORDRAY, P, FAIN, P. R, KEPPEN, L. D, BARKER, D. F

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A mutation causing alport syndrome with tardive hearing loss is common in the Western United States von BARKER, D. F, PRUCHNO, C. J, JIANG, X, ATKIN, C. L, STONE, E. M, DENISON, J. C, FAIN, P. R, GREGORY, M. C

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Evidence for Effective Suppression of Recombination in the Chromosome 17q21 Segment Spanning RNU2–BRCA1 von Liu, Xudong, Barker, David F.

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Paternal origin of new mutations in Von Recklinghausen neurofibromatosis von Jadayel, D, Fain, P, Upadhyaya, M, Ponder, M. A, Huson, S. M, Carey, J, Fryer, A, Mathew, C. G. P, Barker, D. F, Ponder, B. A. J

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Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q von BARKER, D. F, DENISON, J. C, ATKIN, C. L, GREGORY, M. C

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Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1) von Hallam, P. J., Harding, A. E., Berciano, J., Barker, D. F., Malcolm, S.

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A 2D crossover-based map of the human X chromosome as a model for map integration von Chance, Phillip F, Nguyen, Kim, Econs, Michael J, Kort, Edward N, Redd, Douglas F, Fain, Pamela R, Barker, David F

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The BRCA1 and 1A1.3B Promoters Are Parallel Elements of a Genomic Duplication at 17q21 von Barker, David F., Liu, Xudong, Almeida, Eduardo R.A.

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Molecular Dissection of a Contiguous Gene Syndrome: Frequent Submicroscopic Deletions, Evolutionarily Conserved Sequences, and a Hypomethylated "Island" in the Miller-Dieker Chromo... von Ledbetter, David H., Ledbetter, Susan A., VanTuinen, Peter, Summers, Kim M., Robinson, Terence J., Nakamura, Yusuke, Wolff, Roger, White, Ray, Barker, David F., Wallace, Margaret R., Collins, Francis S., Dobyns, William B.

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DNA duplication associated with Charcot-Marie-Tooth disease type 1A von Lupski, James R., de Oca-Luna, Roberto Montes, Slaugenhaupt, Susan, Pentao, Liu, Guzzetta, Vito, Trask, Barbara J., Saucedo-Cardenas, Odila, Barker, David F., Killian, James M., Garcia, Carlos A., Chakravarti, Aravinda, Patel, Pragna I.

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Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas von Baker, Suzanne J., Fearon, Eric R., Nigro, Janice M., Hamilton, Stanley R., Preisinger, Ann C., Jessup, J. Milburn, VanTuinen, Peter, Ledbetter, David H., Barker, David F., Nakamura, Yusuke, White, Ray, Vogelstein, Bert

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Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy von FAIN, P. R, BARKER, D. F, CHANCE, P. F

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Charcot — Marie — Tooth neuropathy type 1A with both duplication and non-duplication von lonasescu, Victor V., lonasescu, Rebecca, Searby, Charles, Barker, David F.

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Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22 von Barker, D.F., CIeverly, J., Fain, P.R.

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Chromosome 17p Deletions and p53 Gene Mutations Associated with the Formation of Malignant Neurofibrosarcomas in von Recklinghausen Neurofibromatosis von Menon, A. G., Anderson, K. M., Riccardi, V. M., Chung, R. Y., Whaley, J. M., Yandell, D. W., Farmer, G. E., Freiman, R. N., Lee, J. K., Li, F. P., Barker, D. F., Ledbetter, D. H., Kleider, A., Martuza, R. L., Gusella, J. F., Seizinger, B. R.

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A genetic map of human chromosome 17p von Wright, E.C., Goldgar, D.E., Fain, P.R., Barker, D.F., Skolnick, M.H.

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