198 related articles for article (PubMed ID: 7573129)
1. Interstitial duplication 19p.
Stratton RF; DuPont BR; Olsen AS; Fertitta A; Hoyer M; Moore CM
Am J Med Genet; 1995 Jul; 57(4):562-4. PubMed ID: 7573129
[TBL] [Abstract][Full Text] [Related]
2. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
[TBL] [Abstract][Full Text] [Related]
3. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
Lindgren V; Rosinsky B; Chin J; Berry-Kravis E
Am J Med Genet; 1994 Jan; 49(1):67-73. PubMed ID: 8172253
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
[TBL] [Abstract][Full Text] [Related]
5. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
[TBL] [Abstract][Full Text] [Related]
6. Characterization of a duplication in the terminal band of 4p by molecular cytogenetics.
Wyandt HE; Milunsky J; Lerner T; Gusella JF; Hou A; MacDonald M; Adekunle S; Milunsky A
Am J Med Genet; 1993 Apr; 46(1):72-6. PubMed ID: 7684190
[TBL] [Abstract][Full Text] [Related]
7. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
Odell JM; Siebert JR; Bradley C; Salk D
Am J Med Genet; 1987 Jul; 27(3):687-92. PubMed ID: 3631140
[TBL] [Abstract][Full Text] [Related]
8. Interstitial duplication of 7(q22-->q34).
Stratton RF; DuPont BR; Mattern VL; Schelonka RL; Moore CM
Am J Med Genet; 1993 Sep; 47(3):380-2. PubMed ID: 8135285
[TBL] [Abstract][Full Text] [Related]
9. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
[TBL] [Abstract][Full Text] [Related]
10. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7.
Lopez-Rangel E; Hrynchak M; Friedman JM
Am J Med Genet; 1993 Sep; 47(3):326-9. PubMed ID: 8135275
[TBL] [Abstract][Full Text] [Related]
11. Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.
Sillén A; Wadelius C; Annerén G
Am J Med Genet; 1998 Nov; 80(2):163-8. PubMed ID: 9805135
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.
Skrypnyk C; Goecke TO; Majewski F; Bartsch O
Am J Med Genet; 2002 Nov; 113(2):207-12. PubMed ID: 12407714
[TBL] [Abstract][Full Text] [Related]
13. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
Knoll JH; Asamoah A; Pletcher BA; Wagstaff J
Am J Med Genet; 1995 Jan; 55(2):221-4. PubMed ID: 7717422
[TBL] [Abstract][Full Text] [Related]
14. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
Gibson LH; McGrath J; Yang-Feng TL
Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
[TBL] [Abstract][Full Text] [Related]
15. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
Behjati F; Shafaghati Y; Firouzabadi SG; Kahrizi K; Bagherizadeh I; Najmabadi H; Bint S; Ogilvie C
Eur J Med Genet; 2008; 51(6):608-14. PubMed ID: 18674645
[TBL] [Abstract][Full Text] [Related]
16. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.
López-Exposito I; Guillén-Navarro E; Bafallíu JA; Bernabé MC; Escalona A; Fuster C
Eur J Med Genet; 2006; 49(6):511-5. PubMed ID: 16824814
[TBL] [Abstract][Full Text] [Related]
17. Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.
Rosenfeld W; Verma RS; Jhaveri RC; Estrada R; Evans H; Dosik H
Am J Med Genet; 1981; 10(2):187-92. PubMed ID: 7315875
[TBL] [Abstract][Full Text] [Related]
18. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
Cappon SL; Duncan AM; Khalifa MM
Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
Taysi K; Dengler DR; Jones LA; Heersma JR
Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
[No Abstract] [Full Text] [Related]
20. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.
Melnyk AR; Dewald G
Am J Med Genet; 1994 Mar; 50(1):12-4. PubMed ID: 7512788
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
