These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
98 related articles for article (PubMed ID: 3742852)
21. 46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3. Surana RB; Braudo ME; Conen PE; Slade RH Clin Genet; 1977 Mar; 11(3):201-6. PubMed ID: 837571 [No Abstract] [Full Text] [Related]
22. Reciprocal translocation with special reference to reproductive failure. Subrt I Hum Genet; 1980; 55(3):303-7. PubMed ID: 7203462 [TBL] [Abstract][Full Text] [Related]
23. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation. Sekhon GS; Taysi K; Rath R Hum Genet; 1978 Oct; 44(1):99-103. PubMed ID: 711241 [TBL] [Abstract][Full Text] [Related]
24. Bilateral nephroblastoma associated with a 3;17 translocation. Soulie J; Rousseau-Merck MF; Mouly H; Nezelof C Cytogenet Cell Genet; 1985; 39(1):64-6. PubMed ID: 2983951 [TBL] [Abstract][Full Text] [Related]
25. A family with severe X-linked arthrogryposis. Hennekam RC; Barth PG; Van Lookeren Campagne W; De Visser M; Dingemans KP Eur J Pediatr; 1991 Jul; 150(9):656-60. PubMed ID: 1915520 [TBL] [Abstract][Full Text] [Related]
26. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q. Larson LM; Wasdahl WA; Saumur JH; Coleman ML; Hall JG; Dolan CR; Schutta CJ Clin Genet; 1982 Mar; 21(3):187-95. PubMed ID: 7094394 [TBL] [Abstract][Full Text] [Related]
28. Familial translocation, t(2;5) (p23; g31). Osztovics M; Kiss P Clin Genet; 1975 Aug; 8(2):112-6. PubMed ID: 1175316 [TBL] [Abstract][Full Text] [Related]
29. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]
30. Partial 3q trisomy due to an unbalanced 3/10 translocation. Blumberg B; Moore R; Mohandas T Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658 [TBL] [Abstract][Full Text] [Related]
31. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11). Murthy DS; Patel ZM; Ambani LM Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504 [TBL] [Abstract][Full Text] [Related]
32. An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12. Sachdeva S; Smith GF; Justice P J Med Genet; 1974 Sep; 11(3):303-5. PubMed ID: 4139264 [TBL] [Abstract][Full Text] [Related]
33. Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: report of a second family. Di Rocco M; Reboa E; Barabino A; Larnaout A; Canepa M; Savioli C; Cremonte M; Borrone C Am J Med Genet; 1990 Oct; 37(2):237-40. PubMed ID: 2248291 [TBL] [Abstract][Full Text] [Related]
34. Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance. Rosenmann A; Arad I J Med Genet; 1974 Mar; 11(1):91-4. PubMed ID: 4837288 [TBL] [Abstract][Full Text] [Related]
35. Partial trisomy 12q associated with a familial translocation. Hemming L; Brown R Clin Genet; 1979 Jul; 16(1):25-8. PubMed ID: 477011 [TBL] [Abstract][Full Text] [Related]
36. A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2. Kobayashi H; Baumbach L; Matise TC; Schiavi A; Greenberg F; Hoffman EP Hum Mol Genet; 1995 Jul; 4(7):1213-6. PubMed ID: 8528211 [TBL] [Abstract][Full Text] [Related]
37. 16q trisomy in a family with a balanced 15/16 translocation. Schmickel R; Poznanski A; Himebaugh J Birth Defects Orig Artic Ser; 1975; 11(5):229-36. PubMed ID: 1218219 [No Abstract] [Full Text] [Related]
38. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation. Fried K; Bar-Yochai A; Rosenblatt M; Mundel G J Med Genet; 1978 Feb; 15(1):76-8. PubMed ID: 633321 [TBL] [Abstract][Full Text] [Related]
39. [Congenital multiple arthrogryposis. Clinical and genetic study]. Gallegos-Rivera M; Carnevale A; Valdés H; del Castillo V Bol Med Hosp Infant Mex; 1991 Feb; 48(2):88-95. PubMed ID: 2054091 [TBL] [Abstract][Full Text] [Related]
40. [Familial occurrence of translocation between chromosomes No. 3 and 4]. Balícek P; Zizka J Cas Lek Cesk; 1979 Jan; 118(3):73-6. PubMed ID: 427853 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]