177 related articles for article (PubMed ID: 4782671)
1. Cytogenetic study of a 5-14 translocation in man.
Borgaonkar DS; Blair SM; Lutz JB; Kelly T; Tice RR; Delaney NV; Hutchinson JR; Bias WB
J Hered; 1973; 64(5):299-300. PubMed ID: 4782671
[No Abstract] [Full Text] [Related]
2. A familial Y-autosome translocation in man.
Noel B; Emerit I; Luciani JM; Quack B
Clin Genet; 1971; 2(1):1-6. PubMed ID: 5111751
[No Abstract] [Full Text] [Related]
3. Cytogenetic study of individuals suspected of chromosome anomalies.
Singh DN
Clin Pediatr (Phila); 1977 Jul; 16(7):619-22. PubMed ID: 862299
[No Abstract] [Full Text] [Related]
4. 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]
5. Karyotype with chromosomal abnormality with various inherited defects in the offspring (recombination aneusomy).
Warter S; Ruch JV; Lehmann M
Humangenetik; 1973 Dec; 20(4):355-9. PubMed ID: 4768111
[No Abstract] [Full Text] [Related]
6. Tandem duplication (5q13 to 22) in a mentally deficient girl.
Kessel E; Pfeiffer RA
Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177
[TBL] [Abstract][Full Text] [Related]
7. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
Allderdice PW; Miller OJ; Miller DA; Breg WR; Gendel E; Zelson C
Humangenetik; 1971; 13(3):205-9. PubMed ID: 5114675
[No Abstract] [Full Text] [Related]
8. A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.
Andersen O; Lundsteen C; Niebuhr E
Cytogenet Cell Genet; 1981; 30(1):3-10. PubMed ID: 7261680
[TBL] [Abstract][Full Text] [Related]
9. Inherited partial duplication of chromosome No. 15.
Fujimoto A; Towner JW; Ebbin AJ; Kahlstrom EJ; Wilson MG
J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
[TBL] [Abstract][Full Text] [Related]
10. [Translocation of a part of the long arms of chromosome 5 on the long arms of a D group chromosome (Bq-,Dq+) in a child and its mother].
Rumpler Y; Ruch JV; Beauvais P
Humangenetik; 1967; 4(2):166-73. PubMed ID: 6078180
[No Abstract] [Full Text] [Related]
11. Ring (15) chromosome.
Yunis E; Leibovici M; Quintero L
Hum Genet; 1981; 57(2):207-9. PubMed ID: 7228035
[TBL] [Abstract][Full Text] [Related]
12. A familial reciprocal translocation between three chromosomes.
Creasy MR; Crolla JA; Daker MG
Humangenetik; 1974; 24(4):303-8. PubMed ID: 4140839
[No Abstract] [Full Text] [Related]
13. Inheritance of a ring 14 chromosome.
Riley SB; Buckton KE; Ratcliffe SG; Syme J
J Med Genet; 1981 Jun; 18(3):209-13. PubMed ID: 7241544
[TBL] [Abstract][Full Text] [Related]
14. A family showing transmission of a translocation t(3porq-;Cq+).
McHugh J; Wright T; Cooke P
J Med Genet; 1971 Dec; 8(4):509-12. PubMed ID: 5149535
[No Abstract] [Full Text] [Related]
15. Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm.
Bernstein R; Milne AT; Jenkins T
J Med Genet; 1978 Aug; 15(4):310-4. PubMed ID: 712764
[TBL] [Abstract][Full Text] [Related]
16. Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12.
Mayeda K; Weiss L; Lindahl R; Dully M
Am J Hum Genet; 1974 Jan; 26(1):59-64. PubMed ID: 4811755
[No Abstract] [Full Text] [Related]
17. Chromosome banding patterns in an infant with 13q minus syndrome.
Ikeuchi T; Sonta S; Sasaki M; Hujita M; Tsunematsu K
Humangenetik; 1974 Mar; 21(4):309-14. PubMed ID: 4134627
[No Abstract] [Full Text] [Related]
18. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
Miller JQ
Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
[No Abstract] [Full Text] [Related]
19. 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]
20. Chromosome 15 abnormality in a mentally retarded adult.
Kelly S; Almy R; Dagle A
J Med Genet; 1969 Dec; 6(4):438-41. PubMed ID: 5365954
[No Abstract] [Full Text] [Related]
[Next] [New Search]
