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3. [Dermatoglyphics in medicine]. Sharets IuD Vestn Akad Med Nauk SSSR; 1973; 28(7):61-9. PubMed ID: 4274403 [No Abstract] [Full Text] [Related]
4. [Children with chromosome abnormalities in a pediatric department]. Nielsen J; Friedrich U; Holm V; Sveinsson S Ugeskr Laeger; 1973 Feb; 135(8):408-15. PubMed ID: 4265917 [No Abstract] [Full Text] [Related]
5. A liveborn case of 49,XXXY, + 18. Kardon NB; Berger AL; Elice M; Davis JG; Jenkins EC J Med Genet; 1980 Oct; 17(5):389-90. PubMed ID: 7194375 [TBL] [Abstract][Full Text] [Related]
6. Distribution of sex chromosomes in dysgenetic gonads of mixed type. Röpke A; Kalinski T; Mohnike K; Sel S; Jakubiczka S; Pelz AF; Roessner A; Wieacker PF Cytogenet Genome Res; 2007; 116(1-2):146-51. PubMed ID: 17268195 [TBL] [Abstract][Full Text] [Related]
7. Trisomy of chromosome 16 in a neonate, 47XY,?16+. Taylor AI J Med Genet; 1971 Mar; 8(1):123-5. PubMed ID: 5098068 [No Abstract] [Full Text] [Related]
9. A child with double trisomy: 48,XYY,+18. Felding I; Kristoffersson U Hereditas; 1981; 95(1):169-71. PubMed ID: 7333871 [No Abstract] [Full Text] [Related]
10. Noonan syndrome and trisomy 21 mongolism in sibs. Bianchine JW Am J Dis Child; 1973 Dec; 126(6):823-6. PubMed ID: 4271368 [No Abstract] [Full Text] [Related]
11. Presence of Turner stigmata in a case of dysgenetic male pseudohermaphroditism with 45,X/46,X+mar karyotype. Hashimoto H; Maruyama H; Koshida R; Okuda N; Murayama K; Katsumi T; Watanabe K; Sato T Arch Dis Child; 1997 Mar; 76(3):268-71. PubMed ID: 9135271 [TBL] [Abstract][Full Text] [Related]
12. The phenotype and gonadal histology in XO-XY mosaic individuals: report of two personal cases. Van Campenhout J; Lord J; Vauclair R; Lanthier A; Berard M J Obstet Gynaecol Br Commonw; 1969 Jul; 76(7):631-9. PubMed ID: 5793899 [No Abstract] [Full Text] [Related]
13. Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic-karyotypic correlations. Simpson JL Birth Defects Orig Artic Ser; 1975; 11(4):23-59. PubMed ID: 1098702 [No Abstract] [Full Text] [Related]
14. Chromosome abnormalities and intrauterine growth retardation. Reisman LE Pediatr Clin North Am; 1970 Feb; 17(1):101-10. PubMed ID: 4246127 [No Abstract] [Full Text] [Related]
15. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p. Leichtman LG; Zackowski JL; Storto PD; Newlin A Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648 [TBL] [Abstract][Full Text] [Related]
16. [Chromosome aberration and mental retardation]. Asaka A Shinkei Kenkyu No Shimpo; 1972 Apr; 16(2):226-31. PubMed ID: 4260444 [No Abstract] [Full Text] [Related]
17. Y-21 translocation with gonadal and renal dysgenesis and cardiac rupture. Hillman LS; Sekhon GS; Kaufman RL; Ho CK Am J Dis Child; 1974 Oct; 128(4):560-3. PubMed ID: 4416920 [No Abstract] [Full Text] [Related]
18. Germ cells and ova in dysgenetic gonads of a 46-XY female dizygotic twin. Cussen LJ; MacMahon RA Am J Dis Child; 1979 Apr; 133(4):373-5. PubMed ID: 433851 [TBL] [Abstract][Full Text] [Related]
19. 49,XXYY, +18 in a liveborn male. Webb GC; Krumins EJ; Leversha MA; Ford GW J Med Genet; 1984 Jun; 21(3):232. PubMed ID: 6748025 [No Abstract] [Full Text] [Related]