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Journal De Mycologie Medicale|July 17, 2013
[Isolation of Geosmithia argillacea in a cystic fibrosis patient]F Labbé, S Babchia, F Evreux, et al.Clinical Chemistry|October 1, 1978
Modified erythrocyte uroporphyrinogen I synthase assay, and its clinical interpretationM W Piepkorn, P Hamernyik, R F LabbéUltrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 26, 1998
Cystic hygroma as an early first-trimester ultrasound marker for recurrent Fryns' syndromeI M Hösli, S Tercanli, H Rehder, et al.Clinical Genetics|December 1, 1984
Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathologyU Froster-Iskenius, W Coerdt, H Rehder, et al.American Journal of Medical Genetics|October 1, 1993
Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findingsU G Froster, H Rehder, W Höhn, et al.European Journal of Pediatrics|December 1, 1984
Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformationsW Grote, H Rehder, D Weisner, et al.Zeitschrift Fur Geburtshilfe Und Neonatologie|September 1, 1996
[Possibilities for false-negative findings in trisomy 21 screening with FISH]B Fritz, B Van Oorschot, E Latta, et al.Clinical Chemistry|March 1, 1983
Liquid-chromatographic profiles of urinary porphyrinsW E Schreiber, V A Raisys, R F LabbéClinical Chemistry|December 10, 1999
Zinc protoporphyrin: A metabolite with a missionR F Labbé, H J Vreman, D K StevensonHeredity|September 21, 2017
Genetic signatures of variation in population size in a native fungal pathogen after the recent massive plantation of its host treeF Labbé, M C Fontaine, C Robin, et al.Pageof 12