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3. [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]
4. The dup(3q) syndrome: report of eight cases and review of the literature. Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873 [TBL] [Abstract][Full Text] [Related]
5. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases]. Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975 [No Abstract] [Full Text] [Related]
8. [Genetic counseling. Apropos of familial transmission of 21-D translocation]. Attal B; Cottin J; Someily I Bull Fed Soc Gynecol Obstet Lang Fr; 1971; 23(4):494-7. PubMed ID: 5153258 [No Abstract] [Full Text] [Related]
9. A family with a presumptive C-F translocation in five generations. Therkelsen AJ; Klinge T; Henningsen K; Mikkelsen M; Schmidt G Ann Genet; 1971 Mar; 14(1):13-21. PubMed ID: 5314290 [No Abstract] [Full Text] [Related]
10. Cytogenetic and clinical findings in some cases of chromosomal disturbances. Zizka J; Balicek P; Lichý J Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1976; 19(3-4):311-7. PubMed ID: 1072525 [No Abstract] [Full Text] [Related]
11. [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]
12. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)]. Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122 [No Abstract] [Full Text] [Related]
13. 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]
14. [A patient with ring chromosome 13]. Hammond A; Bijlsma JB Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723 [No Abstract] [Full Text] [Related]
15. Brief clinical report: the dup(17p) syndrome. Feldman GM; Baumer JG; Sparkes RS Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295 [TBL] [Abstract][Full Text] [Related]
16. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child]. Walbaum R; Dupuis C; Dehaene P; Delmas-Marsalet Y Ann Genet; 1968 Mar; 11(1):53-5. PubMed ID: 5301757 [No Abstract] [Full Text] [Related]
17. Infant male with ring chromosome 14. Triolo O; Serra A; Bova R; Carlo Stella N; Caruso P Ann Genet; 1981; 24(4):236-8. PubMed ID: 6977306 [No Abstract] [Full Text] [Related]
18. 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]