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2. Anatomical studies of a boy trisomic for the distal portion of 13q. Pettersen JC Am J Med Genet; 1979; 4(4):383-400. PubMed ID: 539604 [TBL] [Abstract][Full Text] [Related]
4. Analysis of 137 cases of the trisomy-D syndrome. Lazyuk GI; Kravtosova GI; Kulazhenko VP; Usova YuI ; Usoev SS Sov Genet; 1974 Jan; 7(10):1338-49. PubMed ID: 4824841 [No Abstract] [Full Text] [Related]
5. [Trisomy of the chromosome 13 in a child with multiple malformations]. Adámek R; Kaspárková Z; Kaláb Z; Bílek O; Sekanina Z; Frána L Cesk Pediatr; 1974 Jan; 29(1):49-51. PubMed ID: 4452141 [No Abstract] [Full Text] [Related]
6. Autosomal trisomy 18 and 13 syndromes in Ibadan, Nigeria. Adeyokunnu AA Afr J Med Med Sci; 1983 Jun; 12(2):81-9. PubMed ID: 6322555 [TBL] [Abstract][Full Text] [Related]
7. [Mosaic 14 trisomy in a female child with multiple abnormalities]. Rethoré MO; Couturier J; Carpentier S; Ferrand J; Lejeune J Ann Genet; 1975 Mar; 18(1):71-4. PubMed ID: 1080041 [TBL] [Abstract][Full Text] [Related]
8. [Apropos of trisomy 18 - a study of 4 observations]. Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124 [No Abstract] [Full Text] [Related]
12. [Ocular and general abnormalities in classical trisomy]. Cagianut B; Molz G; Theiler K Bull Mem Soc Fr Ophtalmol; 1972; 85(0):45-51. PubMed ID: 4211534 [No Abstract] [Full Text] [Related]
13. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations. Wilson WG; Shires MA; Willson KA; Wyandt HE; Harris LM; Kelly TE Am J Med Genet; 1983 Sep; 16(1):131-6. PubMed ID: 6638063 [TBL] [Abstract][Full Text] [Related]
14. [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)]. Castel Y; Rivière D; Boycly JY; Toudic L Ann Genet; 1976 Mar; 19(1):15-9. PubMed ID: 1084116 [TBL] [Abstract][Full Text] [Related]
15. [Partial trisomy of the proximal part of the long arm of chromosome 13]. Saura R; Longy M; Serville F; Sautarel M; Renouil M; Sandler B Pediatrie; 1982 Sep; 37(6):473-7. PubMed ID: 7155728 [No Abstract] [Full Text] [Related]
16. 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]
17. Autosomal chromosome anomalies in man. Taylor AI Med Lab Technol; 1971 Jan; 28(1):66-70. PubMed ID: 4252619 [No Abstract] [Full Text] [Related]
18. 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]
19. [Phenotype and karyotype interrelationships in chromosomal diseases]. Prokof'eva-Bel'govska ; Grinberg KN; Revazov AA; Mikel'saar AV; Kuliev AM Vestn Akad Med Nauk SSSR; 1973; 28(1):37-44. PubMed ID: 4797784 [No Abstract] [Full Text] [Related]
20. Unusual 13/13 translocation and 13 trisomy phenotype. Fryns JP; Kleczkowska A; Kubien E Ann Genet; 1982; 25(2):113-5. PubMed ID: 6984626 [No Abstract] [Full Text] [Related] [Next] [New Search]