Introductory Speech for Dorothy Warburton

Por Jacobs, Patricia A. 
Publicado em 2007

An Analysis of the Break Points of Structural Rearrangements in Man

Por Jacobs, Patricia A., Buckton, Karin E., Cunningham, Catherine, Newton, Marjorie
Publicado em 1974

The XYY Male

Por Brown, W. M. Court, Price, W. H., Jacobs, Patricia A.
Publicado em 1968

Leukaemia Cases with Previous Radiotherapy

Por Baikie, A. G., Brown, W. M. Court, Jacobs, Patricia A.
Publicado em 1961

Duchenne muscular dystrophy (DMD) in a female with an X/autosomal translocation: Further evidence that the DMD locus is at Xp21

Por Jacobs, Patricia A., Hunt, Patricia A., Mayer, Martha, Bart, Robert D.
Publicado em 1981

Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*

Por LEGGETT, VICTORIA, JACOBS, PATRICIA, NATION, KATE, SCERIF, GAIA, BISHOP, DOROTHY V M
Publicado em 2010

Cytogenetic Studies in Acute Leukaemia

Por Baikie, A. G., Jacobs, Patricia A., McBride, J. A., Tough, Ishbel M.
Publicado em 1961

Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure

Por Bennett, Claire E., Conway, Gerard S., Macpherson, James N., Jacobs, Patricia A., Murray, Anna
Publicado em 2010

De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalance

Por Sibbons, Charlene, Morris, Joan K, Crolla, John A, Jacobs, Patricia A, Thomas, N Simon
Publicado em 2012

Expression of the marker(X)(q28) in lymphoblastoid cell lines

Por Jacobs, Patricia A., Hunt, Patricia A., Mayer, Martha, Wang, Jin-Chen, Boss, Gerry R., Erbe, Richard W.
Publicado em 1982

Failure to Find DUP25 in Patients with Anxiety Disorders, in Control Individuals, or in Previously Reported Positive Control Cell Lines

Por Tabiner, Melody, Youings, Sheila, Dennis, Nicholas, Baldwin, David, Buis, Christel, Mayers, Andrew, Jacobs, Patricia A., Crolla, John A.
Publicado em 2003

Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction

Por Hassold, Terry J., Burrage, Lindsay C., Chan, Ernest R., Judis, LuAnn M., Schwartz, Stuart, James, S. Jill, Jacobs, Patricia A., Thomas, N. Simon
Publicado em 2001

Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort

Por Baptista, Julia, Mercer, Catherine, Prigmore, Elena, Gribble, Susan M., Carter, Nigel P., Maloney, Viv, Thomas, N. Simon, Jacobs, Patricia A., Crolla, John A.
Publicado em 2008

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency

Por Murray, Anna, Schoemaker, Minouk J., Bennett, Claire E., Ennis, Sarah, Macpherson, James N., Jones, Michael, Morris, Danielle H., Orr, Nick, Ashworth, Alan, Jacobs, Patricia A., Swerdlow, Anthony J.
Publicado em 2014

Autism, language and communication in children with sex chromosome trisomies

Por Bishop, Dorothy V M, Jacobs, Patricia A, Lachlan, Katherine, Wellesley, Diana, Barnicoat, Angela, Boyd, Patricia A, Fryer, Alan, Middlemiss, Prisca, Smithson, Sarah, Metcalfe, Kay, Shears, Deborah, Leggett, Victoria, Nation, Kate, Scerif, Gaia
Publicado em 2010

Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study

Por Murray, Anna, Bennett, Claire E., Perry, John R.B., Weedon, Michael N., Consortium, ReproGen, Jacobs, Patricia A., Morris, Danielle H., Orr, Nicholas, Schoemaker, Minouk J., Jones, Michael, Ashworth, Alan, Swerdlow, Anthony J.
Publicado em 2011

Segmental Aneuploidy and the Genetic Gross Structure of the Drosophila Genome

Por Lindsley, Dan L., Sandler, L., Baker, Bruce S., Carpenter, Adelaide T. C., Denell, R. E., Hall, Jeffrey C., Jacobs, Patricia A., Miklos, George L. Gabor, Davis, Brian K., Gethmann, R. C., Hardy, R. W., Hessler, A., Miller, Steven M., Nozawa, Hiroshi, Parry, Dilys M., Gould-Somero, M.
Publicado em 1972

Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia

Por Li, Yilong, Schwab, Claire, Ryan, Sarra, Papaemmanuil, Elli, Robinson, Hazel M., Jacobs, Patricia, Moorman, Anthony V., Dyer, Sara, Borrow, Julian, Griffiths, Mike, Heerema, Nyla A., Carroll, Andrew J., Talley, Polly, Bown, Nick, Telford, Nick, Ross, Fiona M., Gaunt, Lorraine, McNally, Richard J. Q., Young, Bryan D., Sinclair, Paul, Rand, Vikki, Teixeira, Manuel R., Joseph, Olivia, Robinson, Ben, Maddison, Mark, Dastugue, Nicole, Vandenberghe, Peter, Stephens, Philip J., Cheng, Jiqiu, Van Loo, Peter, Stratton, Michael R., Campbell, Peter J., Harrison, Christine J.
Publicado em 2014

Fragile X Premutation Is a Significant Risk Factor for Premature Ovarian Failure: The International Collaborative POF in Fragile X Study—Preliminary Data

Por Allingham-Hawkins, Diane J., Babul-Hirji, Riyana, Chitayat, David, Holden, Jeanette J.A., Yang, Kathy T., Lee, C., Hudson, R., Gorwill, H., Nolin, Sarah L., Glicksman, Anne, Jenkins, Edmund C., Brown, W. Ted, Howard-Peebles, Patricia N., Becchi, Cindy, Cummings, Emilie, Fallon, Lee, Seitz, Suzanne, Black, Susan H., Vianna-Morgante, Angela M., Costa, Silvia S., Otto, Paulo A., Mingroni-Netto, Regina C., Murray, Anna, Webb, J., MacSwinney, F., Dennis, N., Jacobs, Patricia A., Syrrou, Maria, Georgiou, Ioannis, Patsalis, Phillipos C., Uzielli, Maria L. Giovannucci, Guarducci, S., Lapi, E., Cecconi, A., Ricci, U., Ricotti, G., Biondi, C., Scarselli, B., Vieri, F.
Publicado em 1999