166 related articles for article (PubMed ID: 7985987)
1. Chromosomal mosaicism limited to fibroblasts and MCA/MR syndrome with fetal hypokinesia of central nervous origin.
Fryns JP; Legius E; Van den Berghe H
Ann Genet; 1994; 37(2):94. PubMed ID: 7985987
[No Abstract] [Full Text] [Related]
2. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.
Raffel LJ; Mohandas T; Rimoin DL
Am J Med Genet; 1986 Aug; 24(4):607-11. PubMed ID: 3740095
[TBL] [Abstract][Full Text] [Related]
3. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.
Fryns JP; Kleczkowska A; Decock P; Massa G; van den Berghe H
Ann Genet; 1992; 35(4):234-6. PubMed ID: 1296522
[TBL] [Abstract][Full Text] [Related]
4. 18q- and 18q+ mosaicism in a mentally retarded boy.
Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
[TBL] [Abstract][Full Text] [Related]
5. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
[No Abstract] [Full Text] [Related]
6. Trisomy 9 mosaicism in a girl with multiple malformations.
Diaz-Mares L; Molina B; Carnevale A
Ann Genet; 1990; 33(3):165-8. PubMed ID: 2288462
[TBL] [Abstract][Full Text] [Related]
7. Ring chromosome 16: a new case.
Vianello MG; Cottafava F; Bartoli D; Franzone G; Casazzava R; Gastaldi R
Ann Genet; 1990; 33(1):36-9. PubMed ID: 2195979
[TBL] [Abstract][Full Text] [Related]
8. Ring chromosome 6: twenty years follow-up.
Fryns JP; Kleczkowska A; van den Berghe H
Ann Genet; 1990; 33(3):179. PubMed ID: 2288465
[No Abstract] [Full Text] [Related]
9. Mosaic isochromosome 8p.
Tilstra DJ; Grove M; Spencer AC; Norwood TH; Pagon RA
Am J Med Genet; 1993 Jun; 46(5):517-9. PubMed ID: 8322812
[TBL] [Abstract][Full Text] [Related]
10. Are some multiple congenital anomalies with mental retardation (MCA/MR) the clinical expression of rare autosomal fragile sites?
Stoll C; Bolender C; Geraudel A; Finck S; Alembik Y; Dott B
Genet Couns; 1991; 2(4):211-5. PubMed ID: 1799418
[TBL] [Abstract][Full Text] [Related]
11. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases.
Reynolds JF; Daniel A; Kelly TE; Gollin SM; Stephan MJ; Carey J; Adkins WN; Webb MJ; Char F; Jimenez JF
Am J Med Genet; 1987 Jun; 27(2):257-74. PubMed ID: 3605212
[TBL] [Abstract][Full Text] [Related]
12. Isochromosome-formation in chromosome 9.
Miller K; Arslan-Kirchner M
Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
[TBL] [Abstract][Full Text] [Related]
13. A de novo tandem duplication 15(q21 leads to qter) mosaic.
Yip MY; Parsons A; Hultén M
Clin Genet; 1982 Jul; 22(1):1-6. PubMed ID: 7172470
[No Abstract] [Full Text] [Related]
14. Mosaic supernumerary small ring chromosome.
Fryns JP; van Herck G; van den Berghe H
J Genet Hum; 1981 Jun; 29(2):151-4. PubMed ID: 7328409
[No Abstract] [Full Text] [Related]
15. [Syndrome of multiple abnormalities in a child with mosaicism 46, XY/47, XY, +E].
Balcar-Boroń A; Sawa H; Slowik J; Marcinkowska A; Robińska E
Pediatr Pol; 1977 Oct; 52(10):1161-4. PubMed ID: 583678
[No Abstract] [Full Text] [Related]
16. The Pallister-Killian syndrome in an African individual.
Woodman BF; Jordan MA; Moller LI; Cartwright JD; De Ravel TJ
Genet Couns; 1995; 6(1):33-6. PubMed ID: 7794559
[TBL] [Abstract][Full Text] [Related]
17. Diploid/tetraploid mosaicism in a stillborn infant with prune belly anomaly.
Urioste M; Pinel I; Gomar JL; Skinner C; Martinez-Frias ML
Ann Genet; 1990; 33(1):49-51. PubMed ID: 2195982
[TBL] [Abstract][Full Text] [Related]
18. Trisomy 14 mosaicism syndrome.
Lipson MH
Am J Med Genet; 1987 Mar; 26(3):541-4. PubMed ID: 3565467
[TBL] [Abstract][Full Text] [Related]
19. Neuroblastoma in patients with constitutional chromosomal changes.
Fryns JP
Genet Couns; 1996; 7(1):73. PubMed ID: 8652093
[No Abstract] [Full Text] [Related]
20. [Chromosomal mosaicism in the r (15) syndrome].
Malygina NA; Mutovin GR; Filina NP; Akif'ev AP
Genetika; 1980; 16(11):2029-33. PubMed ID: 7193157
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
