95 related articles for article (PubMed ID: 4676027)
1. A case of tertiary trisomy due to C-C translocation in the mother.
Endo A; Shimada T; Oda Y
Jinrui Idengaku Zasshi; 1972 Sep; 17(1):44-9. PubMed ID: 4676027
[No Abstract] [Full Text] [Related]
2. [Chromosome 8 trisomy in an infant].
Rogóyski A; Babel M; Tronowska TD
Pediatr Pol; 1982; 57(5-6):425-7. PubMed ID: 7155694
[No Abstract] [Full Text] [Related]
3. [C trisomy].
Berger R
Nouv Presse Med; 1972 Apr; 1(14):951-2. PubMed ID: 5026113
[No Abstract] [Full Text] [Related]
4. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
Taysi K; Chao WT; Monaghan N; Monaco MP
Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
[TBL] [Abstract][Full Text] [Related]
5. [Trisomy 10 p. Apropos of a case caused by a maternal translocation].
Stoll C; Willard D
Pediatrie; 1980; 35(3):251-5. PubMed ID: 7393692
[No Abstract] [Full Text] [Related]
6. [12 p trisomy. A new case (author's transl)].
Kubryk N; Prieur M; Borde M
Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558
[No Abstract] [Full Text] [Related]
7. [Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].
de Grouchy J; Emerit I; Aicardi J
Ann Genet; 1969 Jun; 12(2):133-7. PubMed ID: 5308386
[No Abstract] [Full Text] [Related]
8. [Trisomy 10p as a result of familial 10/22 translocation].
Zergollern L; Begovic D; Muzinić D
Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617
[No Abstract] [Full Text] [Related]
9. [Trisomy 4p. A case presentation (author's transl)].
Delgado A; Egüés J; Muñoz M; González Villa P; Bernaola E; del Amo A
An Esp Pediatr; 1981 Oct; 15(4):383-9. PubMed ID: 7337304
[No Abstract] [Full Text] [Related]
10. [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]
11. 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]
12. [Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].
Rott HD; Schwanitz G; Grosse KP
Z Kinderheilkd; 1971; 109(4):293-9. PubMed ID: 5555168
[No Abstract] [Full Text] [Related]
13. [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]
14. [Partial trisomy of chromosome 22 in an infant].
Rogóyski A; Babel M; Tronowska TD
Pediatr Pol; 1983 Jun; 58(6):561-4. PubMed ID: 6646916
[No Abstract] [Full Text] [Related]
15. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
Obry E; Piussan C; Risbourg B; Dutrillaux B
Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599
[TBL] [Abstract][Full Text] [Related]
16. [On three cases of C trisomy].
Lejeune J; Dutrillaux B; Rethoré MO; Berger R; Debray H; Veron P; Gorce F; Grossiord A
Ann Genet; 1969 Mar; 12(1):28-35. PubMed ID: 5306709
[No Abstract] [Full Text] [Related]
17. A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome.
Tommerup N; Nielsen F
Am J Med Genet; 1983 Nov; 16(3):313-21. PubMed ID: 6316787
[TBL] [Abstract][Full Text] [Related]
18. [Partial trisomy E18 (E18 q--) due to a balanced translocation D-E in the mother].
Gleissner M; Schwanitz G; Rott HD
Monatsschr Kinderheilkd (1902); 1970 Jul; 118(7):441-4. PubMed ID: 5515484
[No Abstract] [Full Text] [Related]
19. IV. Application of the principles of genetic counseling.
Summitt RL
J Tenn Med Assoc; 1971 Apr; 64(4):323-32. PubMed ID: 5575761
[No Abstract] [Full Text] [Related]
20. A case of deletion of short arm of chromosome 8.
Leisti J; Aula P
Birth Defects Orig Artic Ser; 1977; 13(3B):187-94. PubMed ID: 890091
[No Abstract] [Full Text] [Related]
[Next] [New Search]