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American Journal of Medical Genetics|July 1, 1985
Differential diagnosis in young women with oligomenorrhea and the pseudo-pseudohypoparathyroidism variant of Albright's hereditary osteodystrophyF Halal, C Van Dop, J LordAmerican Journal of Medical Genetics|January 1, 1980
Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing lossF C Fraser, J R Sproule, F HalalPediatrics|October 1, 1978
Congenital vesicular eruption caused by Haemophilus influenzae type bF Halal, L Delorme, M Brazeau, et al.American Journal of Medical Genetics|March 1, 1990
Distal deletion of chromosome 1q in an adultF Halal, M Vekemans, P Kaplan, et al.American Journal of Medical Genetics|March 1, 1989
A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2qF Halal, M Vekemans, V M Der KaloustianAmerican Journal of Medical Genetics|March 1, 1983
Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome?F C Fraser, S Aymé, F Halal, et al.American Journal of Medical Genetics|May 1, 1983
Intracranial aneurysms: a report of a large pedigreeF Halal, G Mohr, T Toussi, et al.American Journal of Medical Genetics|February 1, 1982
Gastro-cutaneous syndrome: peptic ulcer/hiatal hernia, multiple lentigines/café-au-lait spots, hypertelorism, and myopiaF Halal, M H Gervais, J Baillargeon, et al.Biochimica Et Biophysica Acta|June 19, 1979
[Multiple molecular forms of human plasma butyrylcholinesterase. I. Apparent molecular parameters and broad pattern of the quaternary structure (author's transl)]P MassonCellular and Molecular Neurobiology|February 1, 1991
Structural and functional investigations of cholinesterases by means of affinity electrophoresisP MassonPageof 46