155 related articles for article (PubMed ID: 6842548)
1. Aberrant melanoblast migration associated with trisomy 18 mosaicism.
Chemke J; Rappaport S; Etrog R
J Med Genet; 1983 Apr; 20(2):135-7. PubMed ID: 6842548
[TBL] [Abstract][Full Text] [Related]
2. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
Devriendt K; Matthijs G; Meireleire J; Roelen L; van Buggenhout G; Fryns JP
Genet Couns; 1998; 9(4):283-6. PubMed ID: 9894166
[TBL] [Abstract][Full Text] [Related]
3. Trisomy 12 mosaicism in a 7 year old girl with dysmorphic features and normal mental development.
English CJ; Goodship JA; Jackson A; Lowry M; Wolstenholme J
J Med Genet; 1994 Mar; 31(3):253-4. PubMed ID: 8014979
[TBL] [Abstract][Full Text] [Related]
4. Pigmentary mosaicism of the hyperpigmented type in two half-brothers.
Horn D; Happle R; Neitzel H; Kunze J
Am J Med Genet; 2002 Sep; 112(1):65-9. PubMed ID: 12239723
[TBL] [Abstract][Full Text] [Related]
5. Gene deletion and duplication effects on phenotype and gamma globulin levels.
Rudd NL; Lamarche PH
J Med Genet; 1971 Mar; 8(1):97-106. PubMed ID: 5098075
[No Abstract] [Full Text] [Related]
6. [Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion].
Lucas J; Le Mée F; Picard F; Le Marec B; Junien C
Ann Genet; 1983; 26(3):187-90. PubMed ID: 6606383
[TBL] [Abstract][Full Text] [Related]
7. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence.
Graham DA; Jewitt MM; Fitzgerald PH
Clin Genet; 1992 Jan; 41(1):36-8. PubMed ID: 1633645
[TBL] [Abstract][Full Text] [Related]
8. [Autosomal chromosome aberrations].
Serville F; Battin J
Bord Med; 1971 May; 4(5):1373-416. PubMed ID: 5105683
[No Abstract] [Full Text] [Related]
9. Familial occurrence of trisomy 22.
Uchida IA; Ray M; McRae KN; Besant DF
Am J Hum Genet; 1968 Mar; 20(2):107-18. PubMed ID: 5643178
[No Abstract] [Full Text] [Related]
10. [Trisomy 18].
Berger R
Nouv Presse Med; 1972 Mar; 1(11):745-8. PubMed ID: 5022253
[No Abstract] [Full Text] [Related]
11. [Do all cases of trisomy 18 with long survival (beyond 10 years) show mosaicism in fibroblasts? (author's transl)].
Crippa L; Marcoz JP; Klein D; Bourquin D
J Genet Hum; 1978 Jun; 26(2):145-60. PubMed ID: 670942
[TBL] [Abstract][Full Text] [Related]
12. Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes.
Taibjee SM; Hall D; Balderson D; Larkins S; Stubbs T; Moss C
Clin Exp Dermatol; 2009 Oct; 34(7):823-9. PubMed ID: 19438553
[TBL] [Abstract][Full Text] [Related]
13. A pair of siblings with diastrophic dysplasia and E trisomy mosaicism.
Holmgren G; Jagell S; Lagerkvist B; Nordenson I
Hum Hered; 1984; 34(4):266-8. PubMed ID: 6479995
[TBL] [Abstract][Full Text] [Related]
14. Familial normal-partial trisomy 16 with selective endoreduplication in malformed proband.
Drets ME; Cardoso JH; Delfino AH; Carrau J
Cytogenetics; 1970; 9(5):333-50. PubMed ID: 5501391
[No Abstract] [Full Text] [Related]
15. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
Smith GF; Shear CS; Jalowayski I; Akesson HO
J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
[No Abstract] [Full Text] [Related]
16. A case of familial chromosomal aberration with G group mosaic.
Gedda L; Torrioli-Riggio G; Romei L; Alfieri A; Calabresi F; Del Porto G; Gentile R
Acta Genet Med Gemellol (Roma); 1967 Jan; 16(1):8-20. PubMed ID: 6063938
[No Abstract] [Full Text] [Related]
17. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
[TBL] [Abstract][Full Text] [Related]
18. Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements.
Soler A; Margarit E; Carrió A; Costa D; Queralt R; Ballesta F
J Med Genet; 1999 Apr; 36(4):333-4. PubMed ID: 10227405
[TBL] [Abstract][Full Text] [Related]
19. [Clinical anatomic and histopathological study of ocular signs in 2 cases of mosaicism associated with autosomal 18-21 double trisomy].
Laliam M; Laliam N; Ouadahi MS; Iles S; Ould Larbi L
Bull Mem Soc Fr Ophtalmol; 1972; 85(0):83-90. PubMed ID: 4211332
[No Abstract] [Full Text] [Related]
20. Follow-up of a girl with cleft lip and palate and multiple malformations: trisomy 20 mosaicism.
Strømme P; van der Hagen CB; Haakonsen M; Risberg K; Hennekam R
Scand J Plast Reconstr Surg Hand Surg; 2005; 39(3):178-9. PubMed ID: 16019751
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]