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7. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression]. Frankova YE; Holenova H; Braulke I Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961 [TBL] [Abstract][Full Text] [Related]
8. [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]
9. Partial trisomy 4p with translocation 4p-, 22p+ in the father. Schwanitz G; Grosse KP Ann Genet; 1973 Dec; 16(4):263-6. PubMed ID: 4544090 [No Abstract] [Full Text] [Related]
10. [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]
11. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development. Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Partial trisomy of chromosome 11: a case report. Falk RE; Carrel RE; Valente M; Crandall BF; Sparkes RS Am J Ment Defic; 1973 Jan; 77(4):383-8. PubMed ID: 4706396 [No Abstract] [Full Text] [Related]
14. [9p trisomy syndrome. Two new cases (author's transl)]. Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523 [TBL] [Abstract][Full Text] [Related]
15. [A new case of trisomy 5p]. Antonenko VG; Levina LIa; Chudnova VI Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat]. Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376 [No Abstract] [Full Text] [Related]
18. The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome. Guthrie RD; Aase JM; Asper AC; Smith DW Am J Dis Child; 1971 Nov; 122(5):421-5. PubMed ID: 5129531 [No Abstract] [Full Text] [Related]