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American Journal of Medical Genetics

Volumn 63, Issue 2, 1996, Pages 392-395

A complex, five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspring

(6) Tuck Muller, Cathy M a Varela, Maria b Li, Shibo a Pridjian, Gabriella b Chen, Harold a Wertelecki, Wladimir a

a UNIVERSITY OF SOUTH ALABAMA (United States)

b TULANE UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

CCR; chromosome 10; insertion; intrachromosomal rearrangement; inversion; recombinant chromosome

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 10; CHROMOSOME BREAKAGE; CHROMOSOME INVERSION; CYTOGENETICS; DEVELOPMENTAL DISORDER; GENE INSERTION; GENE REARRANGEMENT; GENETIC RECOMBINATION; HUMAN; PHENOTYPE; PRIORITY JOURNAL; PROGENY;

CHILD; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; GENE REARRANGEMENT; GROWTH DISORDERS; HUMANS; INFANT; MALE; RECOMBINATION, GENETIC;

EID: 2842567394 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/(SICI)1096-8628(19960517)63:2<392::AID-AJMG13>3.0.CO;2-F Document Type: Article

Times cited : (9)

References (7)

1
- 0027202605
- A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization
- Batista DAS, Tuck-Muller CM, Martinez JE, Kearns WG, Pearson PL, Stetten G (1993): A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization. Hum Genet 92:117-121.
- (1993) Hum Genet , vol.92 , pp. 117-121
- Batista, D.A.S.¹ Tuck-Muller, C.M.² Martinez, J.E.³ Kearns, W.G.⁴ Pearson, P.L.⁵ Stetten, G.⁶

2
- 33750208259
- Gardner RJM, Sutherland GR (eds.) Chromosome Abnormalities and Genetic Counseling. Oxford University Press, New York
- Gardner RJM, Sutherland GR (eds.) (1989): In: Chromosome Abnormalities and Genetic Counseling. Oxford Monographs on Medical Genetics, No. 17. Oxford University Press, New York, pp. 93-97.
- (1989) Oxford Monographs on Medical Genetics , Issue.17 , pp. 93-97

3
- 2842590287
- F. Mitelman (ed): S. Karger, Basel
- ISCN (1995): An International System for Human Cytogenetic Nomenclature, F. Mitelman (ed): S. Karger, Basel, pp 36-37, 53-54, 69.
- (1995) An International System for Human Cytogenetic Nomenclature , pp. 36-37

4
- 0019121059
- Complex chromosome rearrangements: Report of a new case and literature review
- Pai GS, Thomas GH, Mahoney W, Migeon BR (1980): Complex chromosome rearrangements: Report of a new case and literature review. Clin Genet 18:436-444.
- (1980) Clin Genet , vol.18 , pp. 436-444
- Pai, G.S.¹ Thomas, G.H.² Mahoney, W.³ Migeon, B.R.⁴

5
- 0027275637
- True telomeric translocation in a baby with the Prader-Willi phenotype
- Reeve A, Norman A, Sinclair P, Whittington-Smith R, Hamey Y, Donnai D, Read A (1993): True telomeric translocation in a baby with the Prader-Willi phenotype. Am J Med Genet 47:1-6.
- (1993) Am J Med Genet , vol.47 , pp. 1-6
- Reeve, A.¹ Norman, A.² Sinclair, P.³ Whittington-Smith, R.⁴ Hamey, Y.⁵ Donnai, D.⁶ Read, A.⁷

6
- 0022259318
- A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome
- Romain DR, Columbano-Green LM, Parfitt RG, Chapman CJ, Smythe RH, Gebbie OB (1985): A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome. Clin Genet 28:166-172.
- (1985) Clin Genet , vol.28 , pp. 166-172
- Romain, D.R.¹ Columbano-Green, L.M.² Parfitt, R.G.³ Chapman, C.J.⁴ Smythe, R.H.⁵ Gebbie, O.B.⁶

7
- 0015246254
- A rapid banding technique for human chromosomes
- Seabright M (1971): A rapid banding technique for human chromosomes. Lancet II:971-972.
- (1971) Lancet , vol.2 , pp. 971-972
- Seabright, M.¹

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