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Literature DB >> 7194847

Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13.

G R Sutherland, L Hinton.

Abstract

Entities: Gene Species

Mesh：

Substances：
Folic Acid
Thymidine

Year: 1981 PMID： 7194847 DOI： 10.1007/bf00282028

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

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7 in total

1. Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors: G R Sutherland
Journal: Am J Hum Genet Date: 1979-03 Impact factor: 11.025

2. The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

Authors: E Donti; G Venti; V Bocchini; G Rosi; R Armellini; N Trabalza
Journal: Hum Genet Date: 1979-04-17 Impact factor: 4.132

3. Heritable fragile sites on human chromosomes. IV. Silver staining.

Authors: G R Sutherland; P Leonard
Journal: Hum Genet Date: 1979 Impact factor: 4.132

4. Constitutional chromosomal breakage.

Authors: F Giraud; S Ayme; J F Mattei; M G Mattei
Journal: Hum Genet Date: 1976-10-28 Impact factor: 4.132

5. More on marker X chromosomes, mental retardation and macro-orchidism.

Authors: P A Jacobs; M Mayer; E Rudak; J Gerrard; E J Ives; M H Shokeir; J Hall; M Jennings; H Hoehn
Journal: N Engl J Med Date: 1979-03-29 Impact factor: 91.245

6. Heritable fragile sites and lymphocyte culture medium containing BrdU.

Authors: J M Scheres; T W Hustinx
Journal: Am J Hum Genet Date: 1980-07 Impact factor: 11.025

7. Heritable fragile sites on human chromosomes. V. A new class of fragile site requiring BrdU for expression.

Authors: G R Sutherland; E Baker; R S Seshadri
Journal: Am J Hum Genet Date: 1980-07 Impact factor: 11.025

7 in total

12 in total

10. Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites.

Authors: G R Sutherland
Journal: Am J Hum Genet Date: 1982-05 Impact factor: 11.025

Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13.

1. Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

2. The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

3. Heritable fragile sites on human chromosomes. IV. Silver staining.

4. Constitutional chromosomal breakage.

5. More on marker X chromosomes, mental retardation and macro-orchidism.

6. Heritable fragile sites and lymphocyte culture medium containing BrdU.

7. Heritable fragile sites on human chromosomes. V. A new class of fragile site requiring BrdU for expression.

1. A BrdU-requiring fragile site on chromosome 12.

2. Studies on three rare fragile sites. 2q13, 12q13, and 17p12 segregating in one family.

3. A new familial "fragile site" on chromosome 16 (q23-24). Cytogenetic and clinical considerations.

4. Fragile site at 12q13 associated with phenotypic abnormalities.

5. Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23.

6. BrdU-sensitive fragile site on long arm of chromosome 16.

7. Familial fragility on chromosome 16 (fra 16q22) enhanced by both interferon and Distamycin A.

8. Autosomal fragile sites and cancer.

9. Chromosome 17 has a real fragile site at p12.

10. Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites.