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Cytogenetic and Genome Research|June 27, 2003
Cloning and expression analysis of SALL4, the murine homologue of the gene mutated in Okihiro syndromeJ Kohlhase, M Heinrich, M Liebers, et al.American Journal of Human Genetics|October 3, 1998
Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated familiesF Goodman, M L Giovannucci-Uzielli, C Hall, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
Basic Science and PathogenesisSoohyun Park, Anthony H Mark, Eilis W Reardon, et al.Development and Psychopathology|July 23, 2014
Viewing relational aggression through multiple lenses: temperament, personality, and personality pathologyJennifer L Tackett, Shauna C Kushner, Kathrin Herzhoff, et al.Journal of Medical Genetics|March 1, 1994
Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qterW Reardon, L van Herwerden, C Rose, et al.Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association|March 10, 2017
Does socioeconomic status mediate racial differences in the cortisol response in middle childhood?Jennifer L Tackett, Kathrin Herzhoff, Avanté J Smack, et al.Archives of Disease in Childhood|April 1, 1992
Anal abnormalities in childhood myotonic dystrophy--a possible source of confusion in child sexual abuseW Reardon, H E Hughes, S H Green, et al.Journal of Medical Genetics|April 1, 1997
Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosisH Fryssira, R Palmer, K A Hallidie-Smith, et al.Nature Genetics|September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeW Reardon, R M Winter, P Rutland, et al.Clinical Dysmorphology|July 12, 2001
Three new European cases of urofacial (Ochoa) syndromeS Garcia-Minaur, F Oliver, J M Yanez, et al.Pageof 16