171 related articles for article (PubMed ID: 5777082)
1. Disappearance of a 47,XX,C+ leucocyte cell line in an infant who had previously exhibited 46,XX-47,XX,C+ mosaicism.
Neu RL; Bargman GJ; Gardner LI
Pediatrics; 1969 Apr; 43(4):623-6. PubMed ID: 5777082
[No Abstract] [Full Text] [Related]
2. [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]
3. Unusual chromosomal mosaic (46, XX-46, XX, Cp+) in a girl with multiple malformations.
Eriksson B; Fraccaro M; Hultén M; Lindsten J; Tiepolo L
Ann Genet; 1968 Mar; 11(1):6-10. PubMed ID: 5301761
[No Abstract] [Full Text] [Related]
4. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
Vigfusson NV; Kapstafer KJ; Lloyd MA
Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. [Study of a 46,XX-46,XX,17r mosaicism].
Petit P; Koulischer L
Ann Genet; 1971 Mar; 14(1):55-8. PubMed ID: 5314296
[No Abstract] [Full Text] [Related]
8. Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis.
Ward BE; Hayden MW; Robinson A
Am J Med Genet; 1988 Dec; 31(4):835-9. PubMed ID: 3239575
[TBL] [Abstract][Full Text] [Related]
9. Mosaic tetrasomy 8p.
Newton D; Hammond L; Wiley J; Kushnick T
Am J Med Genet; 1993 Jun; 46(5):513-6. PubMed ID: 8322811
[TBL] [Abstract][Full Text] [Related]
10. Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46, XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome.
Kotzot D; Schinzel A
Eur J Hum Genet; 2000 Sep; 8(9):709-12. PubMed ID: 10980577
[TBL] [Abstract][Full Text] [Related]
11. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
Badalian LO; Mutovin GR; Malygina NA; Petrukhin AS
Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175
[TBL] [Abstract][Full Text] [Related]
12. Report of a case of 46,xx/45,xx,-20 mosaicism.
Olinici CD
Ann Genet; 1975 Sep; 18(3):206-8. PubMed ID: 1080986
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Diploid-triploid mosaicism: delineation of the syndrome.
Tharapel AT; Wilroy RS; Martens PR; Holbert JM; Summitt RL
Ann Genet; 1983; 26(4):229-33. PubMed ID: 6607703
[TBL] [Abstract][Full Text] [Related]
15. Telomeric tandem translocation tan (14; 15) (q32; q26) and absence of IgA in an incestuous child.
Koulischer L; Lambotte C
Ann Genet; 1974 Sep; 17(3):189-92. PubMed ID: 4548820
[No Abstract] [Full Text] [Related]
16. 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]
17. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
Pettenati MJ; Teot LA; Smith C; Hayworth R; Thomas IT; Veille JC; Rao PN
Am J Med Genet; 1993 Feb; 45(3):365-9. PubMed ID: 8434625
[TBL] [Abstract][Full Text] [Related]
18. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child].
Walbaum R; Dupuis C; Dehaene P; Delmas-Marsalet Y
Ann Genet; 1968 Mar; 11(1):53-5. PubMed ID: 5301757
[No Abstract] [Full Text] [Related]
19. [Chimera 46,XX-69,XXY].
Lejeune J; Salmon C; Berger R; Réthoré MO; Rossier A; Job JC
Ann Genet; 1967 Dec; 10(4):188-92. PubMed ID: 5301691
[No Abstract] [Full Text] [Related]
20. [Chromosome mosaic with 2 aneuploid stem lines in the tissue culture of a patient with multiple abnormalities].
Reinwein H; Schröter R; Wegner G; Wolf U
Helv Paediatr Acta; 1966 Apr; 21(1):72-84. PubMed ID: 5983797
[No Abstract] [Full Text] [Related]
[Next] [New Search]
