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7. [Trisomy of group C (47, XX, C+)]. Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R Arch Fr Pediatr; 1970; 27(10):1081-8. PubMed ID: 5495708 [No Abstract] [Full Text] [Related]
8. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies. Oikawa K; Kajii T; Shimba H; Sasaki M Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379 [No Abstract] [Full Text] [Related]
9. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+). Tal'vik TA; Mikel'saar AV; Mikel'saar RV Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436 [No Abstract] [Full Text] [Related]
10. [Cp trisomy: a new syndrome]. Canu JM; Buentello L; Armendares S Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464 [No Abstract] [Full Text] [Related]
11. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13). Stoll C; Levy JM; Gardea A Humangenetik; 1975; 27(3):269-74. PubMed ID: 1150249 [No Abstract] [Full Text] [Related]
12. Trisomy 9p in a patient with a de novo 9/15 translocation. Jacobsen P; Hobolth N; Mikkelsen M Clin Genet; 1975 Apr; 7(4):317-24. PubMed ID: 1126053 [TBL] [Abstract][Full Text] [Related]
13. A case of trisomy 8 mosaicism 47, xx + 8/46, xx. Aller V; Abrisqueta JA; Perez A; Martin MA; Goday C; Mazo JD Clin Genet; 1975 Mar; 7(3):232-7. PubMed ID: 1139792 [TBL] [Abstract][Full Text] [Related]
14. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family. de Pina Neto JM; Ferrari I Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898 [TBL] [Abstract][Full Text] [Related]
15. Cytogenetics in mentally defective children with anomalies: a controlled study. Summitt RL J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825 [No Abstract] [Full Text] [Related]
16. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example. Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064 [TBL] [Abstract][Full Text] [Related]
17. [Partial C trisomy through translocation t(Cp-;Gp-)]. Deminatti M; Maillard E; Gosselin B; Peltier JM; Bulteel MF; Dupuis C Ann Genet; 1969 Mar; 12(1):36-45. PubMed ID: 5306710 [No Abstract] [Full Text] [Related]
19. Autosomal chromosome aberrations. A review of the clinical syndromes caused by structural chromosome aberrations, mosaic-trisomies 8 and 9, and triploidy. Schinzel A Ergeb Inn Med Kinderheilkd; 1976; 38():37-94. PubMed ID: 782877 [No Abstract] [Full Text] [Related]
20. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father]. Turleau C; De Grouchy J; Roubin M; Chavin-Colin F; Cachin O Ann Genet; 1975 Jun; 18(2):125-9. PubMed ID: 1081365 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]