Indications for chromosome analyses. Determination of clinical criteria to limit the indications for chromosome analysis, a methodological attempt
Grosse, K.P.
Fortschritte der Medizin 95(33): 2013-2018
1977
ISSN/ISBN: 0015-8178 PMID: 914166 Document Number: 112183
Document emailed within 1 workday
Related Documents
Passarge, E. 1978: Indications for chromosome analysis Der Internist 19(8): 445-451Biedermann, K.J. 2001: Indications of fetal chromosome abnormalities in 1st trimester ultrasound Praxis 90(18): 779-783
Ausloos, G. 1996: Indications et contre-indications de l'approche familiale systémique - Indications and contra-indications of systemic family approach P.R.I.S.M.E. Psychiatrie, Recherche et Intervention en Sante Mentale de l'Enfant 6(4): 534-543
Gottlieb, A.B.; Gordon, K.; Giannini, E.H.; Mease, P.; Li, J.; Chon, Y.; Maddox, J.; Weng, H.H.; Wajdula, J.; Lin, S.-L.; Baumgartner, S.W. 2011: Clinical trial safety and mortality analyses in patients receiving etanercept across approved indications Journal of Drugs in Dermatology: Jdd 10(3): 289-300
Novitski, C.E.; Bajer, A.S. 1978: Interaction of microtubules and the mechanism of chromosome movement (zipper hypothesis). 3 Theoretical analysis of energy requirements and computer simulation of chromosome movement Cytobios 18(71-72): 173-182
Ermann, M.; Ermann, G. 1976: Differential indications in the clinical field. Empirical study of management of indications for analytic individual and group psychotherapy respectively in a psychotherayp clinic Zeitschrift für Psychosomatische Medizin und Psychoanalyse 22(4): 342-355
Abramsson, L. 1988: On the investigation of men from infertile relations. A clinical study with special regard to anamnesis, physical examination, semen-, hormone- and chromosome analyses, from men with non-"normal" semen Scandinavian Journal of Urology and Nephrology. Supplementum 113: 1-47
Lovett, M.; Goldgaber, D.; Ashley, P.; Cox, D.R.; Gajdusek, D.C.; Epstein, C.J. 1987: The mouse homolog of the human amyloid beta protein (AD-AP) gene is located on the distal end of mouse chromosome 16: further extension of the homology between human chromosome 21 and mouse chromosome 16 Biochemical and Biophysical Research Communications 144(2): 1069-1075
Schwarzmeier, J.D.; Haas, O.; Paietta, E.; Fischer, P. 1982: Chromosome analysis and TdT determination: important prognostic parameters of blastic crises in chronic myelocytic leukemia Wiener Klinische Wochenschrift 94(19): 514-520
Srsen, S. 1970: Significance of chromosome analysis in clinical practice Bratislavske Lekarske Listy 54(1): 107-120
Li, L.Y.; Xia, J.H.; Dai, H.P.; Xu, F.M.; He, X.X.; Xu, J. 1986: Chromosome analyses of 2,319 cases in genetic counseling clinic Chinese Medical Journal 99(7): 527-534
Niezabitowski, K.; Slowik, T.; Lojek, M. 1971: Attempt at extending indications for sinusography Neurologia i Neurochirurgia Polska 5(4): 555-562
Terzoudi, G.I.; Singh, S.K.; Pantelias, G.E.; Iliakis, G. 2008: Premature chromosome condensation reveals DNA-PK independent pathways of chromosome break repair International Journal of Oncology 33(4): 871-879
Verma, R.S.; Dosik, H.; Wexler, I.B. 1977: Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q Journal de Genetique Humaine 25(4): 295-301
Noutoshi, Y.; Arai, R.; Fujie, M.; Yamada, T. 1997: Designing of plant artificial chromosome (PAC) by using the Chlorella smallest chromosome as a model system Nucleic Acids Symposium Series 37: 143-144
Yakut, S.; Cetin, Z.; Sanhal, C.; Karauzum, S.B.; Karaman, B.; Simsek, M. 2015: Prenatal Diagnosis of de Novo Supernumerary Marker Chromosome Originated from Chromosome 16 by Array-Cgh Genetic Counseling 26(3): 299-305
Sakazume, S. 2014: Spread of X-chromosome inactivation into chromosome 15 is associated with Prader Willi syndrome phenotype in a boy with a t (X ; 15) (p21.1 ; q11.2) translocation No to Hattatsu 46(2): 121-124
Zollinger, A.; Schmid, W.; Vilan, J.; Sorg, B.; Knoblauch, M. 1983: X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism Schweizerische Medizinische Wochenschrift 113(7): 238-244
Prieto, F.; Badia, L.; Mayans, J.; Besalduch, J.; Marty, M.L. 1978: Trysomy of chromosome 1 long arms plus chromosome 9 inversion in leukaemic cells Sangre 23(1): 64-68
Doco-Fenzy, M.; Navrocki, B.; Cornillet, P.; Sabouraud, P.; Robillard, P.; Gruson, N.; Gaillard, D.; Adnet, J.J. 1994: Use of chromosome painting for marker chromosome identification in two children with congenital disorders Bulletin de l'Association des Anatomistes 78(241): 9-13