The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned von Saxena, Richa, Brown, Laura G, Hawkins, Trevor, Alagappan, Raaji K, Skaletsky, Helen, Reeve, Mary Pat, Reijo, Renee, Rozen, Steve, Dinulos, Mary Beth, Disteche, Christine M, Page, David C

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The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome von PARISI, MELISSA A, DINULOS, MARY BETH, LEPPIG, KATHLEEN A, SYBERT, VIRGINIA P, ENG, CHARIS, HUDGINS, LOUANNE

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Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia von Paznekas, William A., Boyadjiev, Simeon A., Shapiro, Robert E., Daniels, Otto, Wollnik, Bernd, Keegan, Catherine E., Innis, Jeffrey W., Dinulos, Mary Beth, Christian, Cathy, Hannibal, Mark C., Jabs, Ethylin Wang

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Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism von GRAF, W. D, UNIS, A. S, YATES, C. M, SULZBACHER, S, DINULOS, M. B, JACK, R. M, DUGAW, K. A, PADDOCK, M. N, PARSON, W. W

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Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty von REIJO, R, SELIGMAN, J, DINULOS, M. B, JAFFE, T, BROWN, L. G, DISTECHE, C. M, PAGE, D. C

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cDNA Cloning and Chromosome Mapping of the Human Fe65 Gene: Interaction of the Conserved Cytoplasmic Domains of the Human β-amyloid Precursor Protein and Its Homologues with the Mo... von Brassler, Steven L., Gray, Matthew D., Sopher, Bryce L., Hu, Qubai, Hearn, Mark G., Pham, Dao G., Dinulos, Mary Beth, Fukuchi, Ken-Ichiro, Sisodia, Sangram S., Miller, Margaret A., Disteche, Christine M., Martin, George M.

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Human Huntingtin Derived from YAC Transgenes Compensates for Loss of Murine Huntingtin by Rescue of the Embryonic Lethal Phenotype von Hodgson, J. Graeme, Smith, Desmond J., McCutcheon, Krista, Koide, H. Brook, Nishiyama, Kazutoshi, Dinulos, Mary Beth, Stevens, Mary E., Bissada, Nagat, Nasir, Jamal, Kanazawa, Ichiro, Disteche, Christine M., Rubin, Edward M., Hayden, Michael R.

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Partial characterization of the genome of nine animal caliciviruses von Matson, D.O, Berke, T, Dinulos, M.B, Poet, E, Zhong, W.M, Dai, X.M, Jiang, X, Golding, B, Smith, A.W

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A New Region of Conservation Is Defined between Human and Mouse X Chromosomes von Dinulos, Mary Beth, Bassi, Maria T., Rugarli, Elena I., Chapman, Verne, Ballabio, Andrea, Disteche, Christine M.

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Isolation, Mapping, and Functional Expression of the Mouse X Chromosome Glycerol Kinase Gene von Huq, A.H.M.Mahbubul, Lovell, Rhonda S., Sampson, Margaret J., Decker, William K., Dinulos, Mary Beth, Disteche, Christine M., Craigen, William J.

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Recent developments with human caliciviruses von DINULOS, MARY BETH, MATSON, DAVID O

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Structure and chromosomal localization of the beta 2 subunit of the human brain sodium channel von Eubanks, J, Srinivasan, J, Dinulos, M B, Disteche, C M, Catterall, WA

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A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related protein von Wang, X, Bornslaeger, E A, Haub, O, Tomihara-Newberger, C, Lonberg, N, Dinulos, M B, Disteche, C M, Copeland, N, Gilbert, D J, Jenkins, N A, Lacy, E

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Mapping of the murine tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes von Disteche, C M, Dinulos, M B, Bassi, M T, Elliott, R W, Rugarli, E I

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Autosomal dominant inheritance of Barber-Say syndrome von Dinulos, Mary Beth, Pagon, Roberta A.

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Introduction: genetic principles, approaches and technologies von Dinulos, Mary Beth

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Expansile bone lesions in a three-generation family von Dinulos, Mary Beth, Sternen, Darci L., Graham, C. Benjamin, Hudgins, Louanne

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Structure and chromosomal localization of the β2 subunit of the human brain sodium channel von Eubanks, James, Srinivasan, Jayashree, Dinulos, Mary Beth, Disteche, Christine M, Catterall, William A

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Structure and chromosomal localization of the beta2 subunit of the human brain sodium channel von Eubanks, J, Srinivasan, J, Dinulos, M B, Disteche, C M, Catterall, W A

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Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes von Martin-Almedina, S, Ogmen, K, Sackey, E, Grigoriadis, D, Karapouliou, C, Nadarajah, N, Ebbing, C, Lord, J, Mellis, R, Kortuem, F, Dinulos, MB, Polun, C, Bale, S, Atton, G, Robinson, A, Reigstad, H, Houge, G, von der Wense, A, Becker, W-H, Jeffery, S, Mortimer, PS, Gordon, K, Josephs, KS, Robart, S, Kilby, MD, Vallee, S, Gorski, JL, Hempel, M, Berland, S, Mansour, S, Ostergaard, P

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