These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
515 related articles for article (PubMed ID: 4413436)
1. 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]
2. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9. Butler LJ; Eades SM; France NE Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708 [No Abstract] [Full Text] [Related]
3. [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]
4. [Partial trisomy C through a familial translocation t(Cq+;Cq-)]. Lejeune J; Rethoré MO; Berger R; Abonyi D; Dutrillaux B; See G Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617 [No Abstract] [Full Text] [Related]
5. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q). Mikkelsen M; Niebuhr E Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712 [No Abstract] [Full Text] [Related]
7. Partial trisomy 9 in the case of familial translocation 8/9 mat. Schwanitz G; Schamberger U; Rott HD; Wieczorek V Ann Genet; 1974 Sep; 17(3):163-6. PubMed ID: 4548816 [No Abstract] [Full Text] [Related]
8. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)]. Turleau C; Grouchy J; Bocquentin F; Roubin M; Colin FC Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037 [TBL] [Abstract][Full Text] [Related]
9. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Cohen MM; Ornoy A; Rosenmann A; Kohn G Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372 [TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23). Kroyer S; Niebuhr E Ann Genet; 1975 Mar; 18(1):50-5. PubMed ID: 50043 [TBL] [Abstract][Full Text] [Related]
11. Trisomy 4p in a family with A t(4;15). Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034 [TBL] [Abstract][Full Text] [Related]
14. Brief cytogenetic report on maternal translocation t(7;9) (p22:p13): two sibs with duplication 9p and one sib with the balanced translocation. Wajntal A; Gonzalez CH; Koiffmann CP; de Souza DH Am J Med Genet; 1985 Feb; 20(2):265-9. PubMed ID: 3976719 [TBL] [Abstract][Full Text] [Related]
15. [2:12 (p25;q21) translocation classed at first as 2/X]. Pasquali F; Zuffardi O; Zamboni G; Bernardi F Ann Genet; 1975 Mar; 18(1):64-6. PubMed ID: 50045 [TBL] [Abstract][Full Text] [Related]
16. [A case of translocation t(Cp-; Bp+)]. Ricci N; Ventimiglia B; Dallapiccola B; Preto G Ann Genet; 1967 Jun; 10(2):82-5. PubMed ID: 5298977 [No Abstract] [Full Text] [Related]
19. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12). Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449 [TBL] [Abstract][Full Text] [Related]
20. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity]. Rethoré MO; Larget-Piet L; Abonyi D; Boeswillwald M; Berger R; Carpentier S; Cruveiller J; Dutrillau B; Lafourcade J; Penneau M; Lejeune J Ann Genet; 1970 Dec; 13(4):217-32. PubMed ID: 5313386 [No Abstract] [Full Text] [Related] [Next] [New Search]