The fallability of X-chromatin as a screening test for anomalies of the X chromosome
Rary, J.M.; Cummings, D.; Jones, H.W.
Obstetrics and Gynecology 51(1): 107-108
1978
ISSN/ISBN: 0029-7844 PMID: 619326 Document Number: 130088
In 13 of 148 patients suspected of anomaies of the X chromosome, the X-chromatin test was misleading. If an anomaly is suspected, a karyotype as well as an X-chromatin study is indicated.
Document emailed within 1 workday
Related Documents
Isshiki, G. 1979: Screening of congenital metabolic anomalies. High risk screening Nihon Rinsho. Japanese Journal of Clinical Medicine Suppl: 1610-1615Rubecz, I.; Kodela, I.; Gasztonyi, V.; Zörényi, I. 1991: Postnatal screening of renal developmental anomalies. Classical diagnostic methods, risk factors and routine screening Orvosi Hetilap 132(11): 585-589
Vrba, M. 1974: The X-chromatin and the chromosome number of the cells from human malignant melanomas of the eye Neoplasma 21(5): 577-581
Nagano, K.; Nishino, T.; Okuda, Y.; Nakayama, M.; Haga, S.; Yamamoto, H. 1994: Structural analysis of the chromatin loop in human chromosome by immunoelectron microscopy Kaibogaku Zasshi. Journal of Anatomy 69(2): 154-160
Kulikov, R.I. 1977: Effect of the y chromosome on the morphology of human F-chromatin under normal and pathological conditions Tsitologiia 19(7): 732-738
Klein, D. 1975: Clinical chromosome anomalies (1st part) Schweizerische Rundschau für Medizin Praxis 64(6): 148-160
Jörgensen, G. 1981: Chromosome anomalies and criminal responsibility Münchener Medizinische Wochenschrift 123(4): 117-118
Jörgensen, G. 1981: Chromosome anomalies and criminal responsibility Münchener Medizinische Wochenschrift 123(4): 117-118
Guillot, M.; Dufier, J.L.; Perignon, F.; Lenoir, G.; de Grouchy, J.; Pinaudeau, Y. 1983: Ocular anomalies in phenotype 46,XY,r(14) (ring chromosome 14) Archives Francaises de Pediatrie 40(5): 433
Breuker, K.H.; Winkhaus-Schindl, I.; Citoler, P. 1978: Chromosome Anomalies in cases of habitual Abortions Geburtshilfe und Frauenheilkunde 38(1): 11-17
Turc-Carel, C.; Mugneret, F.; Sidaner, I. 1983: Constitutional chromosome anomalies and acute leukemia La Semaine des Hopitaux: Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 59(32): 2267-2272
Picardo López, C.; Ramos Corrales, C.; Bello González, J.; Morán Cabré, A.; Sánchez Cascos, A. 1987: Prune belly syndrome with associated anomalies and chromosome changes (20 p+) Anales Espanoles de Pediatria 26(4): 291-294
Rijhsinghani, A.G.; Hruban, R.H.; Stetten, G. 1988: Fetal anomalies associated with an inversion duplication 13 chromosome Obstetrics and Gynecology 71(6 Part 2): 991-994
Angell, R.R.; Hillier, S.G.; West, J.D.; Glasier, A.F.; Rodger, M.W.; Baird, D.T. 1988: Chromosome anomalies in early human embryos Journal of Reproduction and Fertility. Suppl 36: 73-81
Accorsi, A. 1971: Chromosome anomalies in a case of Cornelia de Lange syndrome Minerva Pediatrica 23(25): 1105-1106
Schuler, D.; Ferenczi, I.; Görgényi, A.; Dobos, M.; Fekete, G.; Ruzicska, P. 1972: Chromosome abnormality with unilateral congenital developmental anomalies Orvosi Hetilap 113(27): 1585-1587
Novakov, A.; Vejnović, T. 1997: Modern noninvasive methods for early detection of chromosome anomalies Medicinski Pregled 50(9-10): 353-356
Petit, P.; Van Den Berghe, H. 1979: The 5q- and additional chromosome anomalies in two patients with acute myeloid leukemia Annales de Genetique 22(2): 103-105
Ventruto, V.; Festa, B.; Renda, S.; Stabile, M.; Rinaldi, A.; Rinaldi, M.M.; Cavaliere, M.L.; Lonardo, F.; Garofalo, S. 1983: Phenotype anomalies in subjects with balanced chromosome translocation. Presentation of 4 cases Pathologica 75 Suppl: 258-261
Robinson, A.; Bender, B.G.; Linden, M.G. 1990: Summary of clinical findings in children and young adults with sex chromosome anomalies Birth Defects Original Article Series 26(4): 225-228