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The Journal of Pediatrics|November 1, 1990
Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome)L Jadresic, J Leake, I Gordon, et al.British Medical Journal|March 8, 1980
Population screening for congenital hypothyroidismJ A Hulse, D B Grant, B E Clayton, et al.European Journal of Pediatrics|June 1, 1984
Neonatal hyperparathyroidismC A Dezateux, J C Hyde, H M Hoey, et al.Journal of Neurosurgery|July 1, 1996
Management of childhood craniopharyngioma: can the morbidity of radical surgery be predicted?C J De Vile, D B Grant, B E Kendall, et al.Clinical Genetics|September 1, 1994
Unilateral renal aplasia in X-linked Kallmann's syndromeJ M Kirk, D B Grant, G M Besser, et al.American Journal of Medical Genetics|June 15, 1993
Complete and partial XY sex reversal associated with terminal deletion of 10q: report of 2 cases and literature reviewA O Wilkie, F M Campbell, P Daubeney, et al.Human Molecular Genetics|August 1, 1995
A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasiaL Laue, S M Wu, M Kudo, et al.Archives of Disease in Childhood|June 1, 1993
Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndromeD B Grant, N D Barnes, M Dumic, et al.The Journal of Clinical Investigation|December 1, 1995
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidismS H Pearce, D Trump, C Wooding, et al.Molecular Endocrinology (Baltimore, Md.)|November 17, 1998
Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasiaS M Wu, K M Hallermeier, L Laue, et al.Pageof 14