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Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomaliesP. Franceschini; M. Cirillo Silengo; G. Davi; R. Bianco; M. Biagioli · 1983
Cardiovascular Development and Congenital Malformations (Cardiovascular Development and Congenital Malformations) || Cardiovascular Anomalies in Patients with Deletion 22q11.2: A Multicenter Study in KoreaArtman, Michael; Benson, D. Woodrow; Srivastava, Deepak; Nakazawa, Makoto · 2005
Multiple Congenital Anomalies and Global Developmental Delay in a Patient with Interstitial 6q25.2q26 Deletion: A Diagnostic OdysseyPaulraj, Prabakaran; Palumbos, Janice C.; Openshaw, Amanda; Carey, John C.; Toydemir, Reha M. · Cytogenetic and Genome Research · 2018
Partial 5p Deletion and Partial 5q Duplication in a Patient with Multiple Congenital Anomalies: A Two-Step Mechanism in Chromosomal Rearrangement Mediated by Non-Allelic Homologous RecombinationOu, Zhishuo Z.; Kochmar, Sally; Yatsenko, Svetlana A.; Woerner, Audrey C.; Acquaro, Roxanne; Ortiz, Damara; Surti, Urvashi; Hu, Jie · Cytogenetic and Genome Research · 2018
Neurological Outcome After Traumatic Transverse Sacral FracturesKempen, D.H.R.; Delawi, D.; Altena, M.C.; Kruyt, M.C.; van den Bekerom, M.P.J.; Oner, F.C.; Poolman, R.W. · JBJS Reviews · 2018
Transsymaptic adaptation in skeletal muscle of “myasthenic” ratsMolenaar, Peter C.; Molenaar, P.C.; Van Kempen, G.Th.H.; Oen, B.S. · Journal of Autoimmunity · 1989
IJCS special regional issue on AfricaAlet C Erasmus; Elizabeth Kempen · 2012
UNITED STATES OF AMERICA.Zitman, F.G.; Linssen, A.C.G.; Edelbroek, P.M.; Van Kempen, G.M.J. · The Lancet · 1914
OBITUARYJarry, J.; Schadendorf, D.; Greenwood, C.; Spatz, A.; van Kempen, L.C. · The Lancet · 1947
DERMATOGLYPHICS IN PARTIAL C TRISOMIESJongbloet, P.H.; Van Kempen, C.; Borgaonkar, D.S. · The Lancet · 1968
andvan Bentum, P. J. M.; van Kempen, H.; van de Leemput, L. E. C.; Perenboom, J. A. A. J.; Schreurs, L. W. M.; Teunissen, P. A. A. · Physical Review B · 1987
sat low temperaturesMaior, M. M.; Wiegers, S. A. J.; Penning, F. C.; van Kempen, H.; Maan, J. C. · Physical Review B · 1997
Barth syndromeJefferies, John L. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2013
Congenital microcephalyAlcantara, Diana; O'Driscoll, Mark · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Introduction: Brain malformationsMirzaa, Ghayda M.; Paciorkowski, Alex R. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Pontocerebellar hypoplasiaRudnik-Schöneborn, Sabine; Barth, Peter G.; Zerres, Klaus · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Pallister-Killian syndromeIzumi, Kosuke; Krantz, Ian D. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2014
Cytogenetic highlights and transitionsSpinner, Nancy B. · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016
IntroductionAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016
Publication schedule for 2016American Journal of Medical Genetics Part C: Seminars in Medical Genetics · 2016