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4. Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21. De la Chapelle A; Koivisto M; Schröder J J Med Genet; 1973 Dec; 10(4):384-9. PubMed ID: 4129974 [TBL] [Abstract][Full Text] [Related]
5. Updating advances in cytogenetics. Applications of the new chromosome banding methods. Breg WR Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402 [No Abstract] [Full Text] [Related]
6. Cytogenetic study of a 5-14 translocation in man. Borgaonkar DS; Blair SM; Lutz JB; Kelly T; Tice RR; Delaney NV; Hutchinson JR; Bias WB J Hered; 1973; 64(5):299-300. PubMed ID: 4782671 [No Abstract] [Full Text] [Related]
7. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies. Kakati S; Sinha AK Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026 [No Abstract] [Full Text] [Related]
8. Frequency of deletion of short arm satellites in acrocentric chromosomes. Nielsen J; Friedrich U; Hreidarsson AB J Med Genet; 1974 Jun; 11(2):177-80. PubMed ID: 4135219 [TBL] [Abstract][Full Text] [Related]
9. A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother. Short EM; Solitare GB; Breg WR J Med Genet; 1972 Sep; 9(3):367-73. PubMed ID: 5079109 [No Abstract] [Full Text] [Related]
10. [Chromosomic identification in Robertsonian translocations by a banding technic]. Prieto F; Badía L; Sanz MA; Eslava MT Sangre (Barc); 1973; 18(3):349-55. PubMed ID: 4127965 [No Abstract] [Full Text] [Related]
11. [Familial D-E translocation]. Meyer-Robisch M; Schwanitz G Acta Genet Med Gemellol (Roma); 1967 Oct; 16(4):365-75. PubMed ID: 5593928 [No Abstract] [Full Text] [Related]
12. Frequency and genetic effect of 1qh plus. Nielsen J; Friedrich U; Hreidarsson AB Humangenetik; 1974 Feb; 21(2):193-6. PubMed ID: 4134842 [No Abstract] [Full Text] [Related]
13. [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]
14. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat. Borgaonkar DS; McKusick VA; Farber PA J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973 [TBL] [Abstract][Full Text] [Related]
15. Developments in laboratory diagnosis of chromosomal abnormalities. Frias JL Ann Clin Lab Sci; 1975; 5(5):369-76. PubMed ID: 52330 [TBL] [Abstract][Full Text] [Related]
16. [Gonadal agenesia 46, XX. Presence of a familial double satellite on a chromosome of the D group]. Lucciani JM; Blanc B; Carlon N; Capodano-Wagner AM; Piana L; Stahl A; Serment H Bull Fed Soc Gynecol Obstet Lang Fr; 1970; 22(1):106-10. PubMed ID: 5453535 [No Abstract] [Full Text] [Related]
18. [Value of the use of fluorescent substances in the study of normal and pathologic human karyotypes. I. Identification of the Y chromosome]. Franceschini P; Fabris C; Bogetti G; Santoro MA; Chaippo G Minerva Pediatr; 1972 Jun; 24(21):862-7. PubMed ID: 4114776 [No Abstract] [Full Text] [Related]
19. A family with D-D translocation. Krmpotic E; Ramanathan K; Grossman A J Med Genet; 1968 Sep; 5(3):205-10. PubMed ID: 5708025 [No Abstract] [Full Text] [Related]