Search Results - "Catherwood, Anne"

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  1. 1
    Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints

    Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints by Gajecka, Marzena, Saitta, Sulagna C., Gentles, Andrew J., Campbell, Lindsey, Ciprero, Karen, Geiger, Elizabeth, Catherwood, Anne, Rosenfeld, Jill A., Shaikh, Tamim, Shaffer, Lisa G.

    “…Deletions of chromosome 1p36 are one of the most frequently encountered subtelomeric alterations. Clinical features of monosomy 1p36 include neurocognitive…”
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  2. 2
    High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome

    High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome by Busse, Tracy, Graham Jr, John M., Feldman, Gerald, Perin, Juan, Catherwood, Anne, Knowlton, Robert, Rappaport, Eric F., Emanuel, Beverly, Driscoll, Deborah A., Saitta, Sulagna C.

    Published in Human mutation (01-01-2011)
    “…The 22q11 Deletion Syndrome includes the overlapping phenotypes of DiGeorge/Velocardiofacial Syndromes, characterized by conotruncal heart defects, cleft…”
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  3. 3
    Phenomenes interlinguistiques en acquisition de la L1 bilingue: Etude de cas

    Phenomenes interlinguistiques en acquisition de la L1 bilingue: Etude de cas by Lemay-Catherwood, Marie Anne Lucie

    Published 01-01-2003
    “…This case study's main purpose is to observe and describe interlinguistic phenomena in a French-English bilingual preschooler acquiring both languages…”
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    Dissertation
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