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2. Non-fluorescent Y chromosome. Bühler E Helv Paediatr Acta; 1974; Suppl 34():127. PubMed ID: 4452635 [No Abstract] [Full Text] [Related]
3. Quantitative studies of Y chromosomal fluorescence in human interphase nuclei. Lamborot-Manzur M; Tishler PV; Atkins L Clin Genet; 1972; 3(2):103-15. PubMed ID: 4115478 [No Abstract] [Full Text] [Related]
4. The use of fluorescence techniques for the recognition of mammalian chromosomes and chromosome regions. Caspersson T; Lindsten J; Lomakka G; Moller A; Zech L Int Rev Exp Pathol; 1972; 11():1-72. PubMed ID: 4122097 [No Abstract] [Full Text] [Related]
5. [Identification of several chromosome aberrations in man by the fluorescent method using quinacrine yprite]. Kulikov RI; Mashkova MV; Verlinskaia DK; Bondarev GN Tsitologiia; 1976 Feb; 18(2):213-8. PubMed ID: 59989 [TBL] [Abstract][Full Text] [Related]
6. [Theoretical and clinical problems of the fluorescent chromosome staining method]. Romer TE Pol Tyg Lek; 1972 Feb; 27(9):349-53. PubMed ID: 4111946 [No Abstract] [Full Text] [Related]
7. XX-XO complex of sex chromosomes in a child with an unusual phenotype. Mikel'saar AV; Naidenova MM; Tal'vik TA; Mikel'saar RV; Kaselaid VL; Tsuker EI; Grinberg KN Sov Genet; 1973 Aug; 7(2):250-5. PubMed ID: 4804067 [No Abstract] [Full Text] [Related]
8. [X-chromosome translocations. Examination based on treatment with BUDR and staining with acridine orange]. Dutrillaux B; Laurent C; Gilgenkrantz S; Frédéric J; Carpentier S; Couturier J; Lejeune J Helv Paediatr Acta; 1974; Suppl 34():19-31. PubMed ID: 4141698 [No Abstract] [Full Text] [Related]
9. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes. Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV; Lur'e IV Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425 [No Abstract] [Full Text] [Related]
10. Human cytogenetics: trends and techniques. Porter IH Prog Clin Pathol; 1973; 5():19-48. PubMed ID: 4131375 [No Abstract] [Full Text] [Related]
11. Identificaton of a translocation with quinacrine fluorescence in a patient with acute leukemia. Rowley JD Ann Genet; 1973 Jun; 16(2):109-12. PubMed ID: 4125056 [No Abstract] [Full Text] [Related]
13. [Determination of male nuclear sex in human blood cells]. Mende S; Alonso A Dtsch Med Wochenschr; 1971 Jun; 96(26):1122 passim. PubMed ID: 5558762 [No Abstract] [Full Text] [Related]
14. [Dicentric Yp chromosome as one of the reasons for the absence of fluorescence in human Y chromosome]. Verlinskaia DK; Prozorova MV Tsitologiia; 1983 Jun; 25(6):696-8. PubMed ID: 6684338 [TBL] [Abstract][Full Text] [Related]
15. [Fluorescence microscopy of Y chromatin. A method for the study of Y-chromosome abnormalities]. Nielsen H; Skakkebaek NE; Philip J Ugeskr Laeger; 1971 Apr; 133(14):631-4. PubMed ID: 4102670 [No Abstract] [Full Text] [Related]
16. [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)]. Emerit I; German J; Crippa LP; Sureau C Ann Genet; 1970 Dec; 13(4):245-8. PubMed ID: 5313888 [No Abstract] [Full Text] [Related]
17. [Chromosomal determination of pathological personality development in man]. Firko M; Matuszewicz T; Trembla K Psychiatr Pol; 1971; 5(3):317-24. PubMed ID: 4256510 [No Abstract] [Full Text] [Related]
18. [Apropos of a cas of ring chromosome X]. Deminatti M; Maillard E; Fossati P; Bulteel MF Ann Genet; 1968 Mar; 11(1):56-8. PubMed ID: 5301758 [No Abstract] [Full Text] [Related]
19. Value of fluorescent Y chromosome and sex chromatin tests. Vakil DV; Lewin PK; Conen PE Acta Cytol; 1973; 17(3):220-3. PubMed ID: 4121639 [No Abstract] [Full Text] [Related]
20. Gynecologic and cytogenetic aspects of gonadal agenesis and dysgenesis. Barakat BY; Jones HW Obstet Gynecol; 1970 Sep; 36(3):368-72. PubMed ID: 5451134 [No Abstract] [Full Text] [Related] [Next] [New Search]