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Genetic Counseling (Geneva, Switzerland)|May 3, 2001
Phenotypic variability of Cat-Eye syndromeM J Berends, G Tan-Sindhunata, B Leegte, et al.
The Netherlands Journal of Medicine|December 1, 1992
No constant relationship between islet amyloid polypeptide (IAPP) and insulin expression in insulinomasM G Nieuwenhuis, A D van Mansfeld, J A van Unnik, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 7, 1991
[Neurofibromatosis and a tumor of Vater's papilla]J C de Mol van Otterloo, E C Ooms, C J Lips, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 1, 1990
Detection of calcitonin-encoding mRNA by radioactive and non-radioactive in situ hybridization: improved colorimetric detection and cellular localization of mRNA in thyroid sectionsM Denijn, R A De Weger, M J Berends, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 17, 1999
The importance of family history in young patients with endometrial cancerM J Berends, J H Kleibeuker, E G de Vries, et al.
Scandinavian Journal of Gastroenterology. Supplement|January 5, 2002
Clinical definition of hereditary non-polyposis colorectal cancer: a search for the impossible?M J Berends, Y Wu, R H Sijmons, et al.
Hormone and Metabolic Research. Supplement Series|January 1, 1989
Pheochromocytoma-induced hypertensive encephalopathy revealing MEN-IIa syndrome in a 13-year old boy. Implications for screening procedures and surgeryM Jadoul, J R Leo, M J Berends, et al.
Henry Ford Hospital Medical Journal|January 1, 1992
Long-term follow-up in four large MEN 2 families in The NetherlandsC J Lips, M J Berends, J Brouwers-Smalbraak, et al.
Human Pathology|January 11, 2001
Adrenocortical adenocarcinoma in an MSH2 carrier: coincidence or causal relation?M J Berends, A Cats, H Hollema, et al.
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