1981

ZORA Publication List

Publications

• Statz, A; Boltshauser, Eugen; Schinzel, Albert; Spiess, H (1981). Computed tomography in Pelizaeus-Merzbacher disease. Neuroradiology, 22(2):103-105.
• Schinzel, Albert (1981). Porencephalic cysts as a result of placental damage at amniocentesis?. Archives of Disease in Childhood, 56(5):405.
• Schinzel, Albert; Schmid, Werner; Fraccaro, Marco; Tiepolo, L; Zuffardi, Orsetta; Opitz, John M; Lindsten, Jan; Zetterqvist, P; Enell, H; Baccichetti, C; Tenconi, R; Pagon, Roberta A (1981). The 'Cat Eye syndrome': Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter→q11) associated with a characteristic phenotype. Human Genetics, 57(2):148-158.
• Schinzel, Albert (1981). Particular behavioral symptomatology in patients with rare autosomal chromosome aberrations. In: Symposium of the European Society of Human Genetics, Zurich, Switzerland, 26 März 1981 - 28 März 1981. Elsevier, 195-210.
• Schinzel, Albert (1981). Incomplete trisomy 22 II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13). Human Genetics, 56(3):263-268.
• Schinzel, Albert (1981). Incomplete trisomy 22 III. Mosaic-trisomy 22 and the problem of full trisomy 22. Human Genetics, 56(3):269-273.
• Schinzel, Albert; Schmid, Werner; Auf der Maur, P; Moser, H; Degenhardt, K H; Geisler, M; Grubisic, A (1981). Incomplete trisomy 22 I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families. Human Genetics, 56(3):249-262.
• Schinzel, Albert (1981). Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25). Journal of Medical Genetics, 18(1):64-68.
• Schinzel, Albert (1981). Case Report 78: large head, abnormal genitalia, hypoplastic kidneys, intrauterine growth retardation. In: Feingold, Murray; Buyse, Marylou; Gellis, Sydney S; Paul, Natalie W. Syndrome identification. New York: March of Dimes Birth Defects Foundation, 20-22.
• Schinzel, Albert (1981). Fortschritte der klinischen Zytogenetik. Pädiatrische Fortbildungskurse für die Praxis = Cours de perfectionnement en pédiatrie pour le praticien, (52):42-58.
• Schmid, M; Poppen, A; Schmid, Werner; Engel, W (1981). Somatic pairings of the Y heterochromatin in human XYY and XYqi cells. Cytogenetics and cell genetics, 29(4):203-214.
• Schmid, Werner; Nielsen, Johannes (1981). Human behavior and genetics : proceedings of the Symposium of the European Society of Human Genetics held at the University of Zurich, Switzerland, March 26-28, 1981. Amsterdam: Elsevier/North-Holland Biomedical Press.