272 related articles for article (PubMed ID: 7856655)
21. Duplication 7p de novo and literature review.
Zerres K; Schwanitz G; Gellissen K; Schroers L; Sohler R
Ann Genet; 1989; 32(4):225-9. PubMed ID: 2692511
[TBL] [Abstract][Full Text] [Related]
22. De novo partial 2p duplication with postmortem description.
Monteleone PL; Blair JD; Graviss ER; Chen SC; Salvador A; Grzegocki JA; Monteleone JA
Am J Med Genet; 1981; 10(1):55-64. PubMed ID: 7197468
[TBL] [Abstract][Full Text] [Related]
23. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
[TBL] [Abstract][Full Text] [Related]
24. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
Bode H; Bühler EM; Wyler F; Hadzilselimovic F
Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
[TBL] [Abstract][Full Text] [Related]
25. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
Sarda P; Lefort G; Devaux P; Humeau C; Rieu D
Ann Genet; 1992; 35(2):117-20. PubMed ID: 1524409
[TBL] [Abstract][Full Text] [Related]
26. Partial duplication 16p resulting from a 3:1 segregation of a maternal reciprocal translocation.
Mori MA; Gomar JL; Diaz de Bustamante A; Ananias A; Pinel I; Martinez-Frias ML
Am J Med Genet; 1987 Jan; 26(1):203-6. PubMed ID: 3812563
[TBL] [Abstract][Full Text] [Related]
27. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
Davies J; Voullaire L; Bankier A
Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Partial duplication of distal 17q.
Bridge J; Sanger W; Mosher G; Buehler B; Hearty C; Olney A; Fordyce R
Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
[TBL] [Abstract][Full Text] [Related]
30. Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomalies.
Levin ML; Shaffer LG; Lewis RAp6 ; Gresik MV; Lupski JR
Am J Med Genet; 1995 Jan; 55(1):30-2. PubMed ID: 7702093
[TBL] [Abstract][Full Text] [Related]
31. Inherited partial trisomy 2: 46,XX,1p+;t(1;2) (p36;q31).
Warren RJ; Panizales EG; Cantwell RJ
Birth Defects Orig Artic Ser; 1975; 11(5):177-9. PubMed ID: 1218210
[No Abstract] [Full Text] [Related]
32. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG
Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725
[No Abstract] [Full Text] [Related]
33. 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]
34. Interstitial deletion 1p as a result of a de novo reciprocal 1p;2p translocation.
Hertz JM; Jensen PH
Ann Genet; 1985; 28(4):228-30. PubMed ID: 3879434
[TBL] [Abstract][Full Text] [Related]
35. Terminal deletion 4q in a severely retarded boy.
de Michelena MI; Campos PJ
Am J Med Genet; 1989 Jun; 33(2):228-30. PubMed ID: 2764033
[TBL] [Abstract][Full Text] [Related]
36. Clinical diagnosis of partial duplication 7q.
Bartsch O; Kalbe U; Ngo TK; Lettau R; Schwinger E
Am J Med Genet; 1990 Oct; 37(2):254-7. PubMed ID: 2248294
[TBL] [Abstract][Full Text] [Related]
37. Interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3)).
Mattia FR; Wardinsky TD; Tuttle DJ; Grix A; Smith KA; Walling P
Am J Med Genet; 1992 Nov; 44(5):551-4. PubMed ID: 1481806
[TBL] [Abstract][Full Text] [Related]
38. Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
Nienhaus H; Mau U; Zang KD
Am J Med Genet; 1992 Nov; 44(5):573-5. PubMed ID: 1481811
[TBL] [Abstract][Full Text] [Related]
39. Child with deletion of 4q and duplication of 1q.
Wade J; Morgan T; Allanson J
Am J Med Genet; 1989 Aug; 33(4):553-4. PubMed ID: 2596517
[No Abstract] [Full Text] [Related]
40. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
Pérez-Castillo A; Martin-Lucas MA; Abrisqueta JA
Ann Genet; 1990; 33(2):121-3. PubMed ID: 2241087
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
