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Oncogene|July 20, 1995
Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancerK Amfo, B Neyns, E Teugels, et al.Blood|December 1, 1994
Molecular basis for type 1 antithrombin deficiency: identification of two novel point mutations and evidence for a de novo splice site mutationK Jochmans, W Lissens, T Yin, et al.Human Reproduction (Oxford, England)|December 1, 1996
Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entitiesW Lissens, B Mercier, H Tournaye, et al.Human Reproduction (Oxford, England)|August 1, 1995
The use of epididymal and testicular spermatozoa for intracytoplasmic sperm injection: the genetic implications for male infertilityS J Silber, Z Nagy, J Liu, et al.Pediatric Neurology|May 1, 1993
Pyruvate dehydrogenase deficiency: clinical and biochemical diagnosisL De Meirleir, W Lissens, R Denis, et al.Clinical Pharmacology and Therapeutics|January 1, 1987
Calcium entry blockade or beta-blockade in long-term management of hypertension in blacksJ R M'Buyamba-Kabangu, R Fagard, P Lijnen, et al.Journal of Medical Genetics|September 1, 1994
A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutationsB Mercier, W Lissens, G Novelli, et al.Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.Pediatric Research|December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathyL De Meirleir, W Lissens, C Benelli, et al.Molecular Reproduction and Development|October 30, 2018
BMP4 plays a role in apoptosis during human preimplantation developmentC De Paepe, A Aberkane, D Dewandre, et al.Pageof 19