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Human Mutation|April 29, 1998
An androgen receptor gene mutation (A645D) in a boy with a normal phenotypeA Nordenskjöld, S SöderhällThe Journal of Clinical Endocrinology and Metabolism|September 24, 1998
Molecular characterization of 5 alpha-reductase type 2 deficiency and fertility in a Swedish familyA Nordenskjöld, S A IvarssonHuman Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M AnvretHuman Genetics|February 1, 1994
WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele originA Nordenskjöld, E Friedman, M AnvretLakartidningen|March 9, 2000
[Boy or girl? Molecular mechanisms in sex differentiation]A Wedell, M Ritzén, A NordenskjöldJournal of Virology|July 1, 1970
Deoxyribonucleotide pools and deoxyribonucleic acid synthesis in mouse embryo cells infected with three classes of polyoma virus particlesL Skoog, B A Nordenskjöld, U LindbergJournal of Pediatric Surgery|July 1, 1996
No evidence of WT1 gene mutations in children with congenital diaphragmatic herniaA Nordenskjöld, M Tapper-Persson, M AnvretHuman Reproduction (Oxford, England)|October 21, 1999
No mutations found in candidate genes for dystociaM Algovik, J Lagercrantz, M Westgren, et al.Journal of Pediatric Urology|October 25, 2008
Autologous in vitro cultured urothelium in hypospadias repairM Fossum, J Svensson, G Kratz, et al.Human Genetics|October 1, 1993
Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locusA Nordenskjöld, F Hedborg, H Luthman, et al.Pageof 5