Showing results (11-20 of 494) with videos related to
Sort By:
Pageof 50
American Journal of Medical Genetics|May 15, 1994
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?A Bottani, W P Robinson, C D DeLozier-Blanchet, et al.Cancer Genetics and Cytogenetics|March 15, 1985
Translocation 2;11 and other significant chromosome changes in acute monoblastic leukemia (M5) with clonal evolution: sequential clinical and cytogenetic studiesC D DeLozier-Blanchet, C Cabrol, C Werner-Favre, et al.European Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in SwitzerlandC D DeLozier-Blanchet, J WisserClinical Genetics|December 1, 1995
Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counselingC D Delozier-Blanchet, L Francipane, M A Morris, et al.American Journal of Medical Genetics|June 13, 1997
Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13S Eliez, M A Morris, S Dahoun-Hadorn, et al.Annales De Genetique|January 1, 1984
Simplified chromosome preparations from chorionic villi obtained by choriocentesis or derived from induced abortionsD Pitmon, P Extermann, P Graff, et al.Journal of Autism and Developmental Disorders|March 1, 1990
Two sisters with Rett syndromeC A Haenggeli, J Moura-Serra, C D DeLozier-BlanchetAmerican Journal of Medical Genetics|November 1, 1986
Lethal multiple pterygium syndrome: report of a new case with hydranencephalyA Mbakop, J N Cox, C Störmann, et al.Cancer|April 15, 1988
Differences between subcutaneous and intraperitoneal forms of three human testicular teratocarcinomas in nude miceM Niederberger, C D DeLozier-Blanchet, C E Hedinger, et al.Dermatology (Basel, Switzerland)|January 1, 1993
Melanoma associated with ring chromosome 7S Vollenweider Roten, C D Delozier-Blanchet, I Masouyé, et al.Pageof 50