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23. [t(7q-; 21q-plus) and familial and trisomy 21]. Giraud F; Hartung M; Mattei JF; Mattie MG Ann Genet; 1974 Mar; 17(1):49-53. PubMed ID: 4276449 [No Abstract] [Full Text] [Related]
24. A new translocation between chromosomes in the 6-12 and 21-22 groups. Lord PM; Casey MD; Laurance BM J Med Genet; 1967 Sep; 4(3):169-76. PubMed ID: 5583342 [No Abstract] [Full Text] [Related]
25. [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]
26. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters]. Giovannelli G; Forabosco A; Dutrillaux B Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939 [No Abstract] [Full Text] [Related]
27. Chromosome abnormalities in two cases with bilateral radial element defects. Faed M; Stewart A; Keay AJ J Med Genet; 1969 Sep; 6(3):342-6. PubMed ID: 5345108 [No Abstract] [Full Text] [Related]
30. Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies. Carrel RE; Sparkes RS; Wright SW J Pediatr; 1971 Apr; 78(4):664-72. PubMed ID: 5547823 [No Abstract] [Full Text] [Related]
31. Partial trisomy 7p associated with familial 7p;22q translocation. Larson LM; Wasdahl WA; Jalal SM J Med Genet; 1977 Aug; 14(4):258-61. PubMed ID: 926137 [TBL] [Abstract][Full Text] [Related]
32. Gene deletion and duplication effects on phenotype and gamma globulin levels. Rudd NL; Lamarche PH J Med Genet; 1971 Mar; 8(1):97-106. PubMed ID: 5098075 [No Abstract] [Full Text] [Related]
33. Familial C-G translocation in three relatives associated with severe mental retardation, short stature, unusual dermatoglyphics and other malformations. Yanagisawa S; Hiraoka K J Ment Defic Res; 1971 Jun; 15(2):136-46. PubMed ID: 5559234 [No Abstract] [Full Text] [Related]
34. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities. Gilbert EF; Opitz JM Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761 [No Abstract] [Full Text] [Related]
35. [CHROMOSOME ABNORMALITIES AND HUMAN DISEASES. CONTRIBUTION TO THE ANATOMICAL STUDY OF TRISOMY 13]. LAFOURCADE J; BOCQUET L; CRUVEILLER J; SARAUX H; BERGER R; LEJEUNE J; HUETDEBAROCHEZ Y; TURPIN R Bull Mem Soc Med Hop Paris; 1964 Mar 6-13; 115():383-99. PubMed ID: 14156094 [No Abstract] [Full Text] [Related]
37. [Dermatoglyphics in medicine]. Sharets IuD Vestn Akad Med Nauk SSSR; 1973; 28(7):61-9. PubMed ID: 4274403 [No Abstract] [Full Text] [Related]
38. [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]
39. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi]. Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R Arch Fr Pediatr; 1970; 27(10):1069-79. PubMed ID: 5495707 [No Abstract] [Full Text] [Related]
40. Double autosomal trisomy (trisomy D+G) with mosaicism. Porter IH; Petersen W; Brown CD J Med Genet; 1969 Sep; 6(3):347-8. PubMed ID: 4242069 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]