345 related articles for article (PubMed ID: 12239731)
1. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
Battaglia A; Brothman AR; Carey JC
Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
[TBL] [Abstract][Full Text] [Related]
2. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
Garcia-Heras J; Martin J
Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
[TBL] [Abstract][Full Text] [Related]
3. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
Hirsch B; Baldinger S
Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
[TBL] [Abstract][Full Text] [Related]
4. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
5. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
[TBL] [Abstract][Full Text] [Related]
6. A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion.
Sgardioli IC; Simioni M; Viguetti-Campos NL; Prota JR; Gil-da-Silva-Lopes VL
Gene; 2013 Jul; 523(2):192-4. PubMed ID: 23566844
[TBL] [Abstract][Full Text] [Related]
7. Trisomy 17p11-pter: unbalanced pericentric inversion, inv(17)(p11q25) in two patients, unbalanced translocations t(4;17)(q27;p11) in a newborn and t(4;17) (p16;p11.2) in a fetus.
Lurie IW; Gurevich DB; Binkert F; Schinzel A
Clin Dysmorphol; 1995 Jan; 4(1):25-32. PubMed ID: 7735502
[TBL] [Abstract][Full Text] [Related]
8. A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
Dufke A; Eggermann K; Balg S; Stengel-Rutkowski S; Enders H; Kaiser P
Cytogenet Cell Genet; 2000; 91(1-4):85-9. PubMed ID: 11173836
[TBL] [Abstract][Full Text] [Related]
9. Recombinant chromosome 4 resulting from a maternal pericentric inversion in two sisters presenting consistent dysmorphic features.
Stembalska A; Laczmanska I; Schlade-Bartusiak K; Czemarmazowicz H; Murawski M; Sasiadek M
Eur J Pediatr; 2007 Jan; 166(1):67-71. PubMed ID: 17013597
[TBL] [Abstract][Full Text] [Related]
10. Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24).
Gadzicki D; Baumer A; Wey E; Happel CM; Rudolph C; Tönnies H; Neitzel H; Steinemann D; Welte K; Klein C; Schlegelberger B
Ann Hum Genet; 2006 Nov; 70(Pt 6):958-64. PubMed ID: 17044870
[TBL] [Abstract][Full Text] [Related]
11. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
[TBL] [Abstract][Full Text] [Related]
12. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
13. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
Ayral D; Raudrant D; Charleux JP; Noel B
Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
[TBL] [Abstract][Full Text] [Related]
14. Recombinant chromosome 18 resulting from a maternal pericentric inversion.
Ayukawa H; Tsukahara M; Fukuda M; Kondoh O
Am J Med Genet; 1994 May; 50(4):323-5. PubMed ID: 8209910
[TBL] [Abstract][Full Text] [Related]
15. [Wolf's syndrome due to pericentric inversion of maternal chromosome 4].
de la Flor Bru J; Guitart M
An Esp Pediatr; 1987 Sep; 27(3):205-7. PubMed ID: 3426010
[TBL] [Abstract][Full Text] [Related]
16. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.
Ciuladaite Z; Preiksaitiene E; Utkus A; Kučinskas V
Cytogenet Genome Res; 2014; 144(2):109-13. PubMed ID: 25401700
[TBL] [Abstract][Full Text] [Related]
17. Trisomy chromosome (22)(q13.1-qter) as a result of paternal inversion (22)(p11q13.1) proved using region-specific FISH probes.
Hou JW
Chang Gung Med J; 2005 Sep; 28(9):657-61. PubMed ID: 16323558
[TBL] [Abstract][Full Text] [Related]
18. The 22q distal trisomy syndrome in a recombinant child.
Rivera H; Garcia-Esquivel L; Romo MG; Perez-Garcia G; Martinez y Martinez R
Ann Genet; 1988; 31(1):47-9. PubMed ID: 3258493
[TBL] [Abstract][Full Text] [Related]
19. Familial pericentric inversion of chromosome 8.
Sujansky E; Smith AC; Peakman DC; McConnell TS; Baca P; Robinson A
Am J Med Genet; 1981; 10(3):229-35. PubMed ID: 6171164
[TBL] [Abstract][Full Text] [Related]
20. Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?
Moedjono SJ; Sparkes RS
Ann Genet; 1980; 23(4):235-7. PubMed ID: 6971603
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
