Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma
Evans, D Gareth, Messiaen, Ludwine M, Foulkes, William D, Irving, Rachel E A, Murray, Alexandra J, Perez-Becerril, Cristina, Rivera, Barbara, McDonald-McGinn, Donna M, Stevenson, David A, Smith, Miriam J
Published in Genetics in medicine (01.09.2021)
Published in Genetics in medicine (01.09.2021)
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Journal Article
Melanocortin-1 Receptor Genotype is a Risk Factor for Basal and Squamous Cell Carcinoma
Box, Neil F., Chen, Wei, Sturm, Richard A., Duffy, David L., Irving, Rachel E., Russell, Anne, Griffyths, Lyn R., Parsons, Peter G., Green, Adele C.
Published in Journal of investigative dermatology (01.02.2001)
Published in Journal of investigative dermatology (01.02.2001)
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In vitro and in vivo MMP gene expression localisation by In Situ-RT-PCR in cell culture and paraffin embedded human breast cancer cell line xenografts
Haupt, Larisa M, Thompson, Erik W, Trezise, Ann E O, Irving, Rachel E, Irving, Michael G, Griffiths, Lyn R
Published in BMC cancer (24.01.2006)
Published in BMC cancer (24.01.2006)
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Journal Article
The translation of psychiatric genetic findings to the clinic
Kendall, Kimberley Marie, Duffin, Donna, Doherty, Joanne, Irving, Rachel, Procter, Annie, Walters, James Tynan Rhys
Published in Schizophrenia research (01.05.2024)
Published in Schizophrenia research (01.05.2024)
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Journal Article
SOX5: Lamb–Shaffer syndrome—A case series further expanding the phenotypic spectrum
Edgerley, Katharine, Bryson, Lisa, Hanington, Lucy, Irving, Rachel, Joss, Shelagh, Lampe, Anne, Maystadt, Isabelle, Osio, Deborah, Richardson, Ruth, Split, Miranda, Sansbury, Francis H., Scurr, Ingrid, Stewart, Helen, McNeil, Alisdair, Low, Karen
Published in American journal of medical genetics. Part A (01.05.2023)
Published in American journal of medical genetics. Part A (01.05.2023)
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Journal Article
POU3F3‐related disorder: Defining the phenotype and expanding the molecular spectrum
Rossi, Alessandra, Blok, Lot Snijders, Neuser, Sonja, Klöckner, Chiara, Platzer, Konrad, Faivre, Laurence Olivier, Weigand, Heike, Dentici, Maria L., Tartaglia, Marco, Niceta, Marcello, Alfieri, Paolo, Srivastava, Siddharth, Coulter, David, Smith, Lacey, Vinorum, Kristin, Cappuccio, Gerarda, Brunetti‐Pierri, Nicola, Torun, Deniz, Arslan, Mutluay, Lauridsen, Mathilde F., Murch, Oliver, Irving, Rachel, Lynch, Sally A., Mehta, Sarju G., Carmichael, Jenny, Zonneveld‐Huijssoon, Evelien, Vries, Bert, Kleefstra, Tjitske, Johannesen, Katrine M., Westphall, Ian T., Hughes, Susan S., Smithson, Sarah, Evans, Julie, Dudding‐Byth, Tracy, Simon, Marleen, Binsbergen, Ellen, Herkert, Johanna C., Beunders, Gea, Oppermann, Henry, Bakal, Mert, Møller, Rikke S., Rubboli, Guido, Bayat, Allan
Published in Clinical genetics (01.08.2023)
Published in Clinical genetics (01.08.2023)
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Expanding the phenotypic spectrum of Chromosome 16p13.11 microduplication: A multicentric analysis of 206 patients
Hamad, Asma, Sherlaw-Sturrock, Charlotte A., Glover, Kate, Salmon, Rachel, Low, Karen, Nair, Ramya, Sansbury, Francis H., Rawlins, LettieE, Carmichael, Jenny, Horton, Rachael, Wedderburn, Sarah, Edgerley, Katherine, Irving, Rachel, Callaghan, Mary, Mercer, Catherine, McGowan, Ruth, Robert, Leema, Titheradge, Hannah, Naik, Swati
Published in European journal of medical genetics (01.04.2023)
Published in European journal of medical genetics (01.04.2023)
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Journal Article
SOX5: Lamb-Shaffer syndrome-A case series further expanding the phenotypic spectrum
Edgerley, Katharine, Bryson, Lisa, Hanington, Lucy, Irving, Rachel, Joss, Shelagh, Lampe, Anne, Maystadt, Isabelle, Osio, Deborah, Richardson, Ruth, Split, Miranda, Sansbury, Francis H, Scurr, Ingrid, Stewart, Helen, McNeil, Alisdair, Low, Karen
Published in American journal of medical genetics. Part A (01.05.2023)
Published in American journal of medical genetics. Part A (01.05.2023)
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Pitfalls in healthcare mergers and acquisitions - emerging issues
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