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.
273 related articles for article (PubMed ID: 316677)
1. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)]. Turleau C; Rethoré MO; Junien C; Lejeune J; de Grouchy J Ann Genet; 1979; 22(3):178-81. PubMed ID: 316677 [TBL] [Abstract][Full Text] [Related]
2. Trisomy 7p due to a mosaic normal/dir dup(7)(p13----p22). Syndrome delineation, critical segment assignment, and a comment on duplications. Cantú JM; Rivas F; Ruiz C; Barajas LO; Moller M; Rivera H Ann Genet; 1985; 28(4):254-7. PubMed ID: 3879442 [TBL] [Abstract][Full Text] [Related]
3. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family. de Pina Neto JM; Ferrari I Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898 [TBL] [Abstract][Full Text] [Related]
4. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant. Milunsky JM; Wyandt HE; Huang XL; Kang XZ; Elias ER; Milunsky A Am J Med Genet; 1996 Jan; 61(3):269-73. PubMed ID: 8741873 [TBL] [Abstract][Full Text] [Related]
5. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14). Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374 [TBL] [Abstract][Full Text] [Related]
6. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit. Fryns JP; Kleczkowska A; Decock P; Massa G; van den Berghe H Ann Genet; 1992; 35(4):234-6. PubMed ID: 1296522 [TBL] [Abstract][Full Text] [Related]
7. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation. van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815 [TBL] [Abstract][Full Text] [Related]
8. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes. Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12). Gonzalez CH; Billerbeck AE; Takayama LC; Wajntal A Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example. Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064 [TBL] [Abstract][Full Text] [Related]
13. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father]. Turleau C; De Grouchy J; Roubin M; Chavin-Colin F; Cachin O Ann Genet; 1975 Jun; 18(2):125-9. PubMed ID: 1081365 [TBL] [Abstract][Full Text] [Related]
15. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization. Chen H; Tuck-Muller CM; Batista DA; Wertelecki W Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449 [TBL] [Abstract][Full Text] [Related]
17. Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen. Schuffenhauer S; Kobelt A; Daumer-Haas C; Löffler C; Müller G; Murken J; Meitinger T Am J Med Genet; 1996 Oct; 65(1):56-9. PubMed ID: 8914742 [TBL] [Abstract][Full Text] [Related]
18. A mildly retarded woman with 46,XX/47,XX, + 18 mosaicism. Bensen JT; Steele MW Am J Med Genet; 1985 Oct; 22(2):343-6. PubMed ID: 4050867 [TBL] [Abstract][Full Text] [Related]
19. [Mosaic trisomy 14 due to an iso dicentric chromosome (author's transl)]. Turleau C; de Grouchy J; Cornu A; Turquet M; Millet G Ann Genet; 1980; 23(4):238-40. PubMed ID: 6971604 [TBL] [Abstract][Full Text] [Related]
20. [Increase of LDH A and partial trisomy 11p (author's transl)]. Rethoré MO; Junien C; Aurias A; Couturier J; Dutrillaux B; Kaplan JC; Lejeune J Ann Genet; 1980; 23(1):35-9. PubMed ID: 6965838 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]