Search Results - Sutcliffe, Maxine J.

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  1. 1
    Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia

    Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia by Heerema, Nyla A., Raimondi, Susana C., Anderson, James R., Biegel, Jaclyn, Camitta, Bruce M., Cooley, Linda D., Gaynon, Paul S., Hirsch, Betsy, Magenis, R. Ellen, McGavran, Loris, Patil, Shivanand, Pettenati, Mark J., Pullen, Jeanette, Rao, Kathleen, Roulston, Diane, Schneider, Nancy R., Shuster, Jonathan J., Sanger, Warren, Sutcliffe, Maxine J., van Tuinen, Peter, Watson, Michael S., Carroll, Andrew J

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  2. 2
    A case study of “ disorganized development” and its possible relevance to genetic determinants of aging

    A case study of “ disorganized development” and its possible relevance to genetic determinants of aging by Walker, Richard F., Pakula, Lawrence C., Sutcliffe, Maxine J., Kruk, Patricia A., Graakjaer, Jesper, Shay, Jerry W.

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  3. 3
    Genomic Loss of Heterozygosity (LOH) in Pediatric Ovarian Germ Cell Tumors (OGCT)

    Genomic Loss of Heterozygosity (LOH) in Pediatric Ovarian Germ Cell Tumors (OGCT) by Sutcliffe, Maxine J, Ortega, Rudolfo, Dumont, Doris P, Panchoosingh, Hardeo, Laden, Samuel

    Published in Cancer genetics
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  4. 4
    Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder

    Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder by CRAWFORD, Fiona C, AIT-GHEZALA, Ghania, MORRIS, Mark, SUTCLIFFE, Maxine J, HAUSER, Robert A, SILVER, Archie A, MULLAN, Michael J

    Published in Human genetics
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  5. 5
    EXTREME VARIANT OF ENLARGED HETEROCHROMATIN REGION ON CHROMOSOME 9Q IN A NORMAL CHILD AND MULTIPLE FAMILY MEMBERS

    EXTREME VARIANT OF ENLARGED HETEROCHROMATIN REGION ON CHROMOSOME 9Q IN A NORMAL CHILD AND MULTIPLE FAMILY MEMBERS by Steffensen, Thora S., Gilbert-Barness, Enid, McH. Sandstrom, Mary, Bell, John R., Bryan, Jenny, Sutcliffe, Maxine J.

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  6. 6
    Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX

    Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX by Sutcliffe, Maxine J., Mueller, O. Thomas, Kousseff, Boris G., Dumont, Doris P., McFarland, Julia A., Mawani, Fayaz, Conforto, Danielle, Ranells, Judith D.

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  7. 7
    Mouse chromosome 7

    Mouse chromosome 7 by Rinchik, E M, Saunders, A M, Holdener-Kenny, B, Sutcliffe, M J, Brown, K A, Brown, S D, Peters, J

    Published in Mammalian genome
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  8. 8
    Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

    Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant? by Li, Feng, Shen, Yiping, Köhler, Udo, Sharkey, Freddie H, Menon, Deepa, Coulleaux, Laurence, Malan, Valérie, Rio, Marlène, McMullan, Dominic J, Cox, H, Fagan, Kerry A, Gaunt, Lorraine, Metcalfe, Kay, Heinrich, Uwe, Hislop, Gordon, Maye, Una, Sutcliffe, Maxine, Wu, Bai-Lin, Thiel, Brian D, Mulchandani, Surabhi, Conlin, Laura K, Spinner, Nancy B, Murphy, Kathleen M, Batista, Denise A.S

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