155 related articles for article (PubMed ID: 4279151)
1. A case with 46, XX, del (11) (q21).
Faust J; Vogel W; Löning B
Clin Genet; 1974; 6(2):90-7. PubMed ID: 4279151
[No Abstract] [Full Text] [Related]
2. Ring 1 chromosome and dwarfism--a possible syndrome.
Wolf CB; Peterson JA; LoGrippo GA; Weiss L
J Pediatr; 1967 Nov; 71(5):719-22. PubMed ID: 6054759
[No Abstract] [Full Text] [Related]
3. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
[No Abstract] [Full Text] [Related]
4. A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS.
LUCAS M; KEMP NH; ELLIS JR; MARSHALL R
Ann Hum Genet; 1963 Nov; 27():189-95. PubMed ID: 14081490
[No Abstract] [Full Text] [Related]
5. A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP.
CLARKE G; STEVENSON AC; DAVIES P; WILLIAMS CE
J Med Genet; 1964 Sep; 1(1):27-32. PubMed ID: 14205979
[No Abstract] [Full Text] [Related]
6. Ring chromosome 10:46,XX,r(10)(p15 leads to q26).
Tsukino R; Tsuda N; Dezawa T; Ishii T; Koike M
J Med Genet; 1980 Apr; 17(2):148-50. PubMed ID: 7381872
[TBL] [Abstract][Full Text] [Related]
7. A complex chromosomal rearrangement with formation of a ring 4.
Bobrow M; Joness LF; Clarke G
J Med Genet; 1971 Jun; 8(2):235-9. PubMed ID: 5096548
[No Abstract] [Full Text] [Related]
8. A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations.
van Hemel JO; van Biervliet JP; de Jager-van der Grift PW
Clin Genet; 1975 Sep; 8(3):213-7. PubMed ID: 1175325
[No Abstract] [Full Text] [Related]
9. An abnormal metacentric chromosome in an infant with leprechaunism.
Ferguson-Smith MA; Hamilton W; Ferguson IC; Ellis PM
Ann Genet; 1968 Dec; 11(4):195-200. PubMed ID: 5306360
[No Abstract] [Full Text] [Related]
10. A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.
Nuzzo F; Marini A; Baglioni C; Ford CE; De Carli L; Piceni Sereni L
Cytogenetics; 1968; 7(3):169-82. PubMed ID: 5682897
[No Abstract] [Full Text] [Related]
11. SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214).
Leschot NJ; Slater RM; Joenje H; Becker-Bloemkolk MJ; de Nef JJ
Hum Genet; 1981; 57(2):220-3. PubMed ID: 7228038
[TBL] [Abstract][Full Text] [Related]
12. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
Jacobsen P; Mikkelsen M; Rosleff F
Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395
[No Abstract] [Full Text] [Related]
13. Chromosomal abnormalities in a girl with physical and mental maldevelopment.
Subrt I; Hníková O
Hum Hered; 1970; 20(3):252-9. PubMed ID: 5489883
[No Abstract] [Full Text] [Related]
14. Tandem duplication of 10(q21-q22) in a mentally deficient man.
Reinthaller A
Clin Genet; 1985 Nov; 28(5):394-6. PubMed ID: 4085143
[TBL] [Abstract][Full Text] [Related]
15. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
Mikkelsen M; Dahl G
Cytogenet Cell Genet; 1973; 12(5):357-66. PubMed ID: 4131091
[No Abstract] [Full Text] [Related]
16. Cytological studies on a human ring chromosome.
Cooke P; Gordon RR
Ann Hum Genet; 1965 Nov; 29(2):147-50. PubMed ID: 5863838
[No Abstract] [Full Text] [Related]
17. Familial bird-headed dwarfism (Seckel's syndrome).
Sauk JJ; Litt R; Espiritu CE; Delaney JR
J Med Genet; 1973 Jun; 10(2):196-8. PubMed ID: 4714590
[TBL] [Abstract][Full Text] [Related]
18. A malformed girl with duplication of chromosome 9q.
Nakahori Y; Nakagome Y
J Med Genet; 1984 Oct; 21(5):387-8. PubMed ID: 6502654
[TBL] [Abstract][Full Text] [Related]
19. Ring chromosome 6 in a malformed boy.
Salamanca-Gonez F; Nava S; Armendares S
Clin Genet; 1975 Nov; 8(5):370-5. PubMed ID: 1204234
[TBL] [Abstract][Full Text] [Related]
20. A newly recognized dominantly inherited syndrome: short stature, ocular and articular anomalies, mental retardation.
Matsoukas J; Liarikos S; Giannikas A; Agoropoulos Z; Papachristou G; Soukakos P
Helv Paediatr Acta; 1973 Nov; 28(5):383-6. PubMed ID: 4773219
[No Abstract] [Full Text] [Related]
[Next] [New Search]
