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Annales De Genetique|January 1, 1988
Usefulness of linked DNA probes for prenatal diagnosis of cystic fibrosis: report of a case in a 1:4 risk pregnancyF Fontaine, F Vasseur, J B Savary, et al.Annales De Genetique|January 1, 1996
Multiple familial lipomatosis with polyneuropathy, an inherited dominant conditionC Stoll, Y Alembik, M TruttmannAnnales De Genetique|January 1, 1995
Renal agenesis and trisomy 22: case report and reviewG J Van Buggenhout, J Verbruggen, J P FrynsAnnales De Genetique|December 2, 1998
Contribution of cytogenetics and FISH in the diagnosis of meningiomas. A study of 189 tumorsH Zattara-Cannoni, D Gambarelli, H Dufour, et al.Annales De Genetique|January 1, 1996
High resolution cytogenetic study in schizophreniaM Casacchia, F Brisdelli, S de Cataldo, et al.Annales De Genetique|January 1, 1996
Proliferation kinetics of chorionic villi in chromosomally normal and abnormal spontaneous abortions analyzed by premature chromosome condensation and northern blotK Miller, V Metze, R Wang, et al.Annales De Genetique|January 1, 1996
Mapping of the human holocarboxylase synthetase gene (HCS) to the Down syndrome critical region of chromosome 21q22J L Blouin, G Duriaux Saïl, S E AntonarakisAnnales De Genetique|January 9, 1999
Partial Xp duplication due to a translocation t(X;15) in two male and two female patients: a familial case report and review of the literatureM I Melaragno, M A Ramos, D BrunoniAnnales De Genetique|January 9, 1999
Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1qT Lukusa, G Van Buggenhout, K Devriendt, et al.Annales De Genetique|January 1, 1995
DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A reviewS Demczuk, A AuriasPageof 129