47,XXY Klinefelter's syndrome and familial marker chromosomes (double satellite on a chromosome of group D)
Luciani, J.M.; Stahl, A.; Jubelin, J.; Simonin, R.
La Semaine des Hopitaux Organe Fonde Par l'Association d'Enseignement Medical des Hopitaux de Paris 46(40): 2524-2528
1970
ISSN/ISBN: 0037-1777 PMID: 4319067 Document Number: 27401
Document emailed within 1 workday
Related Documents
Vdovichenko, Z.V.; Zlatskaia, A.V.; Ternovskaia, T.K. 2001: New morphological marker for chromosomes of the fourth homologous group of Triticinae Tsitologiia i Genetika 35(1): 28-33Taniwaki, M. 1985: New chromosome banding techniques with base specific antibiotics and fluorochromes for qualified identification of marker chromosomes in leukemia and related disorders Nihon Ketsueki Gakkai Zasshi: Journal of Japan Haematological Society 48(6): 1423-1439
Froland, A. 1972: Klinefelter's syndrome. Severe hypogonadism in a phenotypic man with extra X-chromosome material in the cell nuclei Ugeskrift for Laeger 134(45): 2395
Zizka, J.; Balícek, P. 1975: Double trisomy: Down's syndrome and Klinefelter's syndrome Ceskoslovenska Pediatrie 30(9): 414-416
Burden, M.; Lupaşcu, E.; Mărgineanu, L. 1973: A familial case of 17 r ring-shaped chromosome of group e with transmission from father to son Revista Medico-Chirurgicala a Societatii de Medici Si Naturalisti Din Iasi 77(2): 353-357
Alvarez de Santos, M.; Hurtado Ramírez, M.B.; Santos Flores, J.R. 1980: Hypogonadism: Klinefelter's syndrome and mosaicism of Klinefelter Ginecologia y Obstetricia de Mexico 47(280): 101-110
Wenger, S.L.; Surti, U.; Nwokoro, N.A.; Steele, M.W. 1994: Cytogenetic characterization of cat eye syndrome marker chromosome Annales de Genetique 37(1): 33-36
Luciani, J.M.; Mattei, A.; Devictor-Vuillet, M.; Rubin; Stahl, A.; Vague, J. 1970: Study of meiotic chromosomes in a caseof Klinefelter'sdisease with spermatogenesis and 46,XY-47,XXY karyotype Annales de Genetique 13(4): 249-253
Vorsanova, S.G.; Vekhova, N.V.; Solov'ev, I.V.; Kazantseva, L.Z.; Troitskaia, L.A.; Iurov, I.B. 1998: A familial case of mental retardation syndrome linked to fragile X chromosome Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 98(5): 47-49
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
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
Solov'ev, I.V.; Iurov, I.B.; Vorsanova, S.G.; Marcais, B.; Rogaev, E.I.; Kapanadze, B.I.; Brodianskiĭ, V.M.; Iankovskiĭ, N.K.; Roizes, G. 1998: Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization Genetika 34(11): 1470-1479
Midro, A.; Baginska, U. 1979: Behavior of satellite associations of acrocentric chromosomes in women with a history of obstetric-genetic abnormalities Ginekologia Polska 50(3): 251-257
Chen, C.-P.; Lin, S.-P.; Su, J.-W.; Town, D.-D.; Wang, W. 2012: A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1-->p23) associated with attention deficit and hyperactivity disorder Genetic Counseling 23(2): 329-333
Baroncini, A.; Neri, C.; Forabosco, A. 1983: Aarskog's syndrome: study of a new familial group Pathologica 75 Suppl: 153-156
Niedermaier, J.; Moritz, K.B. 2000: Organization and dynamics of satellite and telomere DNAs in Ascaris: implications for formation and programmed breakdown of compound chromosomes Chromosoma 109(7): 439-452
LaForgia, S.; Lasota, J.; Latif, F.; Boghosian-Sell, L.; Kastury, K.; Ohta, M.; Druck, T.; Atchison, L.; Cannizzaro, L.A.; Barnea, G. 1993: Detailed genetic and physical map of the 3p chromosome region surrounding the familial renal cell carcinoma chromosome translocation, t(3;8)(p14.2;q24.1) Cancer Research 53(13): 3118-3124
Mazura, I.; Brdicka, R.; Srám, R.J.; Jurov, J.; Kapras, J. 1989: An alpha-satellite DNA sequence, alpha-RI-6, specific for human chromosomes 13 and 21, detected using the RFLP technic with digoxigenin labelled probes Casopis Lekaru Ceskych 128(40): 1269-1271
Gosden, J.R.; Mitchell, A.R.; Buckland, R.A.; Clayton, R.P.; Evans, H.J. 1975: The location of four human satellite DNAs on human chromosomes Birth Defects Original Article Series 11(3): 168-169
Mispireta, J.L.; Dumont, C.; Cárdenas, M.; de Micheli, A.; Martínez-Ríos, M.A. 1975: Familial occurrence of Wolff-Parkinson-White syndrome. Report of a family group and review of the literature Archivos del Instituto de Cardiologia de Mexico 45(4): 423-434