356 related articles for article (PubMed ID: 6517101)
1. Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss.
Evans MI; White BJ; Kent SG; Levine MA; Levin SW; Larsen JW
Am J Med Genet; 1984 Dec; 19(4):783-90. PubMed ID: 6517101
[TBL] [Abstract][Full Text] [Related]
2. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
Fryns JP; Kleczkowska A; Kenis H
Ann Genet; 1984; 27(1):62-4. PubMed ID: 6609678
[TBL] [Abstract][Full Text] [Related]
3. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
Clark CE; Telfer MA; Cowell HR; Kalamchi A; Steg NL
Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001
[TBL] [Abstract][Full Text] [Related]
4. [Complex rearrangement of chromosomes 3 and 5 in an adolescent with multiple abnormalities].
Naffah J; Der Kaloustian V
Ann Genet; 1975 Jun; 18(2):121-4. PubMed ID: 242250
[TBL] [Abstract][Full Text] [Related]
5. Successive spontaneous abortions with diverse chromosomal aberrations in human translocation heterozygote.
Kohn G; Ornoy A; Ben-Tsur Z; Sadovsky E; Cohen MM
Teratology; 1975 Dec; 12(3):283-9. PubMed ID: 1198335
[TBL] [Abstract][Full Text] [Related]
6. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.
Jenkins EC; Curcuru-Giordano FM; Krishna SG; Cantarella J
Ann Genet; 1975 Jun; 18(2):117-20. PubMed ID: 1081364
[TBL] [Abstract][Full Text] [Related]
7. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
Rivera H; Rivas F; Plascencia L; Cantú JM
Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
[TBL] [Abstract][Full Text] [Related]
8. Frequency and association of NOR's in a family carrying a pericentric inversion of chromosome 14.
Leal-Garza C; Riojas-Valdés V; Montes de Oca-Luna R; Garza-Chapa R
Rev Invest Clin; 1984; 36(3):283-6. PubMed ID: 6542690
[No Abstract] [Full Text] [Related]
9. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
Cohen MM; Ornoy A; Rosenmann A; Kohn G
Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
[TBL] [Abstract][Full Text] [Related]
10. Parental chromosomal aberrations associated with multiple abortions and an abnormal infant.
Hsu LY; Barcinski M; Shapiro LR; Valderrama E; Gertner M; Hirschhorn K
Obstet Gynecol; 1970 Nov; 36(5):723-30. PubMed ID: 5474003
[No Abstract] [Full Text] [Related]
11. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
12. Postzygotic D/D translocation homozygosity associated with recurrent abortions.
Maeda T; Ohno M; Takada M; Matsunobu A; Arai M
Am J Med Genet; 1983 Jul; 15(3):389-92. PubMed ID: 6881208
[TBL] [Abstract][Full Text] [Related]
13. Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.
Papenhausen PR; Mueller OT; Johnson VP; Sutcliffe M; Diamond TM; Kousseff BG
Am J Med Genet; 1995 Nov; 59(3):271-5. PubMed ID: 8599348
[TBL] [Abstract][Full Text] [Related]
14. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
Curry CJ; Ying KL; O'Lague P; Tsai J
Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110
[No Abstract] [Full Text] [Related]
15. 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]
16. [Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].
Scarinci R; Anichini C; Vivarelli R; Berardi R; Pucci L; Rosaia L; Tomaccini D
Boll Soc Ital Biol Sper; 1992 Mar; 68(3):175-81. PubMed ID: 1389073
[TBL] [Abstract][Full Text] [Related]
17. Presumably balanced translocations involving the same band of chromosome No. 4 found in two mentally retarded, dysmorphic individuals.
Skovby F; Niebuhr E
Ann Genet; 1974 Dec; 17(4):243-9. PubMed ID: 4141591
[No Abstract] [Full Text] [Related]
18. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S
Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085
[TBL] [Abstract][Full Text] [Related]
19. [Proximal monosomy 13].
Geormăneanu M; Geormăneanu C
Ann Genet; 1990; 33(3):176-8. PubMed ID: 2288464
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal abnormalities in couples with recurrent abortions.
Low PS; Tay JS; Tan MA; Chua TS; Wong HB
J Singapore Paediatr Soc; 1989; 31(1-2):72-4. PubMed ID: 2770260
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
