186 related articles for article (PubMed ID: 4050855)
21. Trisomy 16p in a liveborn infant and review of trisomy 16p.
O'Connor TA; Higgins RR
Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
[TBL] [Abstract][Full Text] [Related]
22. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
Leichtman LG; Zackowski JL; Storto PD; Newlin A
Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648
[TBL] [Abstract][Full Text] [Related]
23. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
Legare JM; Sekhon GS; Laxova R
Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.
Rutledge JC; Friedman JM; Harrod MJ; Currarino G; Wright CG; Pinckney L; Chen H
Am J Med Genet; 1984 Oct; 19(2):255-64. PubMed ID: 6507477
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
Yu CW; Chen H; Baucum RW; Hand AM
Ann Genet; 1981; 24(3):158-61. PubMed ID: 6974525
[TBL] [Abstract][Full Text] [Related]
29. Duplication of distal 15q: report of five new cases from two different translocation kindreds.
Lacro RV; Jones KL; Mascarello JT; Jones OW; Wilson N; Jones MC
Am J Med Genet; 1987 Mar; 26(3):719-28. PubMed ID: 3565485
[TBL] [Abstract][Full Text] [Related]
30. 2q35qter duplication syndrome: phenotypic definition.
Grammatico P; Di Rosa C; Rinaldi R; Roccella M; Cupilari F; Sbezzi T; Del Porto G
Genet Couns; 1997; 8(4):327-34. PubMed ID: 9457503
[TBL] [Abstract][Full Text] [Related]
31. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
32. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM
Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399
[TBL] [Abstract][Full Text] [Related]
33. Deletion of the distal long arm of chromosome 1: a definable syndrome.
Johnson VP; Heck LJ; Carter GA; Flom JO
Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
[TBL] [Abstract][Full Text] [Related]
34. Familial translocation 5;14 resulting in an unbalanced offspring.
Park JP; Edwards MJ; Moeschler JB; Marin-Padilla JM; Berg SZ; Wurster-Hill DH
Am J Med Genet; 1991 Jun; 39(3):362-6. PubMed ID: 1867291
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
Kennerknecht I; Barbi G; Rodens K
Am J Med Genet; 1993 Dec; 47(8):1157-60. PubMed ID: 7507296
[TBL] [Abstract][Full Text] [Related]
37. Familial t(4;13) with abnormal offspring in three generations.
Najafzadeh TM; Littman VA; Dumars KW
Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065
[TBL] [Abstract][Full Text] [Related]
38. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. DiGeorge anomaly in an infant with deletion of chromosome 22 and dup(9p) due to adjacent type II disjunction.
el-Fouly MH; Higgins JV; Kapur S; Sankey BJ; Matisoff DN; Costa-Fox M
Am J Med Genet; 1991 Mar; 38(4):569-73. PubMed ID: 2063901
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]