561 related articles for article (PubMed ID: 7315873)
1. The dup(3q) syndrome: report of eight cases and review of the literature.
Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Further delineation of the dup(3q) syndrome.
Wilson GN; Dasouki M; Barr M
Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
[TBL] [Abstract][Full Text] [Related]
4. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
Steinbach P; Wolf M; Schmidt H
Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
[TBL] [Abstract][Full Text] [Related]
5. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
[TBL] [Abstract][Full Text] [Related]
6. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM
Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
[TBL] [Abstract][Full Text] [Related]
7. Duplication 3p syndrome: report of a new case and review of the literature.
Charrow J; Cohen MM; Meeker D
Am J Med Genet; 1981; 8(4):431-6. PubMed ID: 7246613
[TBL] [Abstract][Full Text] [Related]
8. The 18p- syndrome. Report of five cases.
Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
[TBL] [Abstract][Full Text] [Related]
9. Duplication 11 (q21 to 23 leads to qter) syndrome.
Francke U; Weber F; Sparkes RS; Mattson PD; Mann J
Birth Defects Orig Artic Ser; 1977; 13(3B):167-86. PubMed ID: 890090
[No Abstract] [Full Text] [Related]
10. 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]
11. 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]
12. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.
Mohammed FM; Farag TI; Gunawardana SS; al-Digashim DD; al-Awadi SA; al-Othman SA; Sundareshan TS
Am J Med Genet; 1989 Mar; 32(3):353-5. PubMed ID: 2729356
[TBL] [Abstract][Full Text] [Related]
13. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
[No Abstract] [Full Text] [Related]
14. Brief clinical report: the dup(17p) syndrome.
Feldman GM; Baumer JG; Sparkes RS
Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295
[TBL] [Abstract][Full Text] [Related]
15. The cytogenetic and clinical implications of a ring chromosome 2.
Cote GB; Katsantoni A; Deligeorgis D
Ann Genet; 1981; 24(4):231-5. PubMed ID: 6977305
[TBL] [Abstract][Full Text] [Related]
16. Duplication-deficiency of the short arm of chromosome 8 following artificial insemination.
Weleber RG; Verma RS; Kimberling WJ; Fieger HG; lubs HA
Ann Genet; 1976 Dec; 19(4):241-7. PubMed ID: 1087853
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Apparently nonmosaic trisomy 22: clinical report and review.
Sundareshan TS; Naguib KK; al-Awadi SA; Redha MA; Hamoud MS
Am J Med Genet; 1990 May; 36(1):7-10. PubMed ID: 2185636
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A patient with partial duplication 2q and partial deficiency 11q.
Ho CK; Henderson KC; Bowyer FP; Eilers KB; Andrews LG
Am J Med Genet; 1987 Nov; 28(3):575-9. PubMed ID: 3322008
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
