96 related articles for article (PubMed ID: 414334)
1. [Clinical and cytogenetic considerations on a case of monosomy 21 in (45, XX-21/46,XY) mosaicism].
Butnariu J; Olinici CD; Popescu A; Giurgiuman M
Rev Pediatr Obstet Ginecol Pediatr; 1977; 26(4):331-6. PubMed ID: 414334
[No Abstract] [Full Text] [Related]
2. De novo partial monosomy 21 with unusual karyotype.
Al-Awadi SA; Naguib KK; Teebi AS; Sundareshan TS
Jinrui Idengaku Zasshi; 1986 Mar; 31(1):45-8. PubMed ID: 3735757
[No Abstract] [Full Text] [Related]
3. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi].
Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R
Arch Fr Pediatr; 1970; 27(10):1069-79. PubMed ID: 5495707
[No Abstract] [Full Text] [Related]
4. Mosaic 45,xy,-21/46,xy in a child with G deletion syndrome I.
Olinici CD; Butnariu J; Popescu A; Giurguiman M
Ann Genet; 1977 Jun; 20(2):115-7. PubMed ID: 302684
[TBL] [Abstract][Full Text] [Related]
5. Monosomy 21: a possible stepwise evolution of the karyotype.
Abeliovich D; Carmi R; Karplus M; Bar-Ziv J; Cohen MM
Am J Med Genet; 1979; 4(3):279-86. PubMed ID: 574719
[TBL] [Abstract][Full Text] [Related]
6. Ring chromosome 21. Observation in a female infant.
Carlo Stella N; Barberi I; Corrado F; Triolo O
Ann Genet; 1984; 27(4):249-51. PubMed ID: 6335374
[TBL] [Abstract][Full Text] [Related]
7. Frequency of chromosomal aberrations in newborn infants with multiple developmental defects.
Chebotarev AN
Sov Genet; 1974 Sep; 8(10):1329-30. PubMed ID: 4439048
[No Abstract] [Full Text] [Related]
8. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
Ferrier S; Freund M; Grétillat A
Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928
[No Abstract] [Full Text] [Related]
11. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
Hustinx TW; Haar BG; Scheres JM; Rutten FJ
Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
[No Abstract] [Full Text] [Related]
12. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
Jalal SM; Martin JA; Benjamin TR; Kukolich MK; Townsend-Parcham JK
Ann Genet; 1990; 33(3):173-5. PubMed ID: 2288463
[TBL] [Abstract][Full Text] [Related]
13. "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]
14. [The Edwards syndrome: a clinical report of a case with thrisomie XXY and mosaicism XX/XY (author's transl)].
Donatuti G; Fasola V; Messana A
Quad Sclavo Diagn; 1977 Dec; 13(4):468-77. PubMed ID: 614607
[No Abstract] [Full Text] [Related]
15. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
Lambotte C; Carlier G; Frederic J; Keutgen J
Acta Paediatr Belg; 1971; 25(2):119-26. PubMed ID: 5565831
[No Abstract] [Full Text] [Related]
16. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
Oikawa K; Kajii T; Shimba H; Sasaki M
Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379
[No Abstract] [Full Text] [Related]
17. [Monosomy C with mosaicism and thymic dysplasia].
Bigliocchi A; Mattioli P; Ciarla MV; Madonna V
Pediatria (Napoli); 1976 Jun; 84(2):307-19. PubMed ID: 1018997
[No Abstract] [Full Text] [Related]
18. A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux.
Leung AK; Rudd NL
Am J Med Genet; 1988 Jan; 29(1):43-8. PubMed ID: 3344775
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.
Krasikov N; Takaesu N; Hassold T; Knops JF; Finley WH; Scarbrough P
Am J Med Genet; 1992 Jun; 43(3):554-60. PubMed ID: 1605248
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
