Showing results (31-40 of 92) with videos related to
Sort By:
Pageof 10
International Journal of Pediatric Otorhinolaryngology|June 22, 1999
Evaluation of the use of a questionnaire to detect hearing loss in babies in ChinaV E Newton, X Liu, X Ke, et al.International Journal of Pediatric Otorhinolaryngology|February 27, 2001
Evaluation of the use of a questionnaire to detect hearing loss in Kenyan pre-school childrenV E Newton, I Macharia, P Mugwe, et al.British Journal of Obstetrics and Gynaecology|February 1, 1982
Amniotic fluid acetylcholinesterase: a retrospective and prospective study of the qualitative methodA P Read, S J Fennell, D Donnai, et al.American Journal of Human Genetics|June 1, 1990
Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouseC Foy, V Newton, D Wellesley, et al.Clinical Dysmorphology|January 1, 1992
Fetus with unbalanced translocation involving chromosomes 2 and 11A M Norman, A P Read, A Clark, et al.Cancer Research|December 15, 1994
Deletion mapping on the short arm of chromosome 3 in squamous cell carcinoma of the oral cavityC L Wu, P Sloan, A P Read, et al.Neuromuscular Disorders : NMD|January 1, 1991
X-linked and FSH dystrophies in one familyB R Lecky, J M MacKenzie, A P Read, et al.European Journal of Human Genetics : EJHG|May 30, 2003
Mutations in PAX1 may be associated with Klippel-Feil syndromeJ M McGaughran, A Oates, D Donnai, et al.Journal of Medical Genetics|July 1, 1990
Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?R G Elles, A P Read, K A Hodgkinson, et al.American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.Pageof 10