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Zeitschrift Fur Geburtshilfe Und Perinatologie|October 1, 1981
[Prenatal differential diagnosis in elevated alpha-fetoprotein concentration in the amniotic fluid (author's transl)]M Cremer, W Schmidt, T Voigtländer, et al.Journal of Child Neurology|January 1, 1990
Isolated lissencephaly: report of four patients from two unrelated familiesL Pavone, F Gullotta, G Incorpora, et al.Neurochirurgia|July 1, 1993
[Photoablation using Excimer laser irradiation--a suitable concept for microneurosurgery?]H J König, G Bücker, A Stefanec, et al.Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1987
Granular cell tumors: evidence for heterogeneous tumor cell differentiation. An immunocytochemical studyJ Ulrich, P U Heitz, T Fischer, et al.Der Pathologe|February 6, 1998
[Paraganglioma of the cauda equina]C H Rickert, S Probst-Cousin, H W Schumacher, et al.Journal of Neuropathology and Experimental Neurology|September 16, 1998
Cell death mechanisms in multiple system atrophyS Probst-Cousin, C H Rickert, K W Schmid, et al.Ultrasound 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.Pageof 22