Medical genetics: 1. Clinical teratology in the age of genomics

ανά Polifka, Janine E., Friedman, J.M.
Έκδοση 2002

Teratogenic Effects of `Recreational' Drugs: Increasing the risk of congenital anomalies

ανά Polifka, Janine E., Friedman, J.M.
Έκδοση 1991

Visual Form Perception: A Comparison of Individuals at High Risk for Psychosis, Recent Onset Schizophrenia and Chronic Schizophrenia

ανά Kimhy, D, Corcoran, C, Harkavy-Friedman, JM, Ritzler, B, Javitt, DC, Malaspina, D
Έκδοση 2007

Survival among people with down syndrome: a nationwide population-based study in denmark

ανά Zhu, Jin Liang, Hasle, Henrik, Correa, Adolfo, Schendel, Diana, Friedman, J.M., Olsen, Jørn, Rasmussen, Sonja A.
Τόπος έκδοσης Genet Med (2012)

Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants

ανά Filges, I., Manokhina, I., Peñaherrera, M.S., McFadden, D.E., Louie, K., Nosova, E., Friedman, J.M., Robinson, W.P.
Τόπος έκδοσης Mol Hum Reprod (2015)

Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

ανά Baross, Ágnes, Delaney, Allen D, Li, H Irene, Nayar, Tarun, Flibotte, Stephane, Qian, Hong, Chan, Susanna Y, Asano, Jennifer, Ally, Adrian, Cao, Manqiu, Birch, Patricia, Brown-John, Mabel, Fernandes, Nicole, Go, Anne, Kennedy, Giulia, Langlois, Sylvie, Eydoux, Patrice, Friedman, JM, Marra, Marco A
Έκδοση 2007

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

ανά Friedman, JM, Adam, Shelin, Arbour, Laura, Armstrong, Linlea, Baross, Agnes, Birch, Patricia, Boerkoel, Cornelius, Chan, Susanna, Chai, David, Delaney, Allen D, Flibotte, Stephane, Gibson, William T, Langlois, Sylvie, Lemyre, Emmanuelle, Li, H Irene, MacLeod, Patrick, Mathers, Joan, Michaud, Jacques L, McGillivray, Barbara C, Patel, Millan S, Qian, Hong, Rouleau, Guy A, Van Allen, Margot I, Yong, Siu-Li, Zahir, Farah R, Eydoux, Patrice, Marra, Marco A
Έκδοση 2009

Exome Sequencing and the Management of Neurometabolic Disorders

ανά Tarailo-Graovac, M., Shyr, C., Ross, C.J., Horvath, G.A., Salvarinova, R., Ye, X.C., Zhang, L.-H., Bhavsar, A.P., Lee, J.J.Y., Drögemöller, B.I., Abdelsayed, M., Alfadhel, M., Armstrong, L., Baumgartner, M.R., Burda, P., Connolly, M.B., Cameron, J., Demos, M., Dewan, T., Dionne, J., Evans, A.M., Friedman, J.M., Garber, I., Lewis, S., Ling, J., Mandal, R., Mattman, A., McKinnon, M., Michoulas, A., Metzger, D., Ogunbayo, O.A., Rakic, B., Rozmus, J., Ruben, P., Sayson, B., Santra, S., Schultz, K.R., Selby, K., Shekel, P., Sirrs, S., Skrypnyk, C., Superti-Furga, A., Turvey, S.E., Van Allen, M.I., Wishart, D., Wu, J., Wu, J., Zafeiriou, D., Kluijtmans, L., Wevers, R.A., Eydoux, P., Lehman, A.M., Vallance, H., Stockler-Ipsiroglu, S., Sinclair, G., Wasserman, W.W., van Karnebeek, C.D.
Τόπος έκδοσης N Engl J Med (2016)