Constitutional ring chromosomes and tumour suppressor genes.

Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells. Nature (2014) 1.66

Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders. J Med Genet (1993) 1.37

Atypical teratoid rhabdoid brain tumor in an infant with ring chromosome 22. Korean J Pediatr (2014) 0.90

A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. J Med Genet (1994) 0.83

Pathogenesis of vestibular schwannoma in ring chromosome 22. BMC Med Genet (2009) 0.79

Ring chromosome 22: a review of the literature and first report from India. Balkan J Med Genet (2012) 0.78

Metachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22. J Med Genet (1995) 0.78

Dysregulation of FOXG1 by ring chromosome 14. Mol Cytogenet (2015) 0.76

The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes. Genetics (1938) 21.89

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature (1983) 11.57

Tumor suppressor genes. Science (1991) 5.72

Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein. Proc Natl Acad Sci U S A (1987) 3.72

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature (1986) 3.40

Retinoblastoma and subband deletion of chromosome 13. Am J Dis Child (1978) 3.11

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion. Pediatrics (1978) 3.04

A new oncogene in human thyroid papillary carcinomas and their lymph-nodal metastases. Nature (1987) 2.60

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage. Nature (1987) 2.54

Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway. Nature (1990) 2.28

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10. Nature (1987) 2.15

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis. Science (1987) 2.06

Comparative behavior of ring chromosomes. Am J Hum Genet (1970) 1.87

Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli. Nature (1988) 1.54

Some retinoblastomas, osteosarcomas, and soft tissue sarcomas may share a common etiology. Proc Natl Acad Sci U S A (1988) 1.41

[The Dr phenotype: a study of threee cases with a ring D chromosome]. Ann Genet (1968) 1.41

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21. Am J Hum Genet (1992) 1.38

Ring 10 chromosome: 46,XX,r10(p15q26). Hum Genet (1978) 1.37

The 13q- deletion syndrome. J Med Genet (1971) 1.14

Cytological and cytogenetical studies on human meningioma. Cancer Genet Cytogenet (1982) 1.14

Familial papillary carcinoma of the thyroid. Am J Med Genet (1986) 1.13

Molecular genetic analysis of chromosome 22 in 81 cases of meningioma. Cancer Res (1990) 1.13

Familial occurrence of papillary thyroid carcinoma. Cancer (1980) 1.06

Dq-, Dr and retinoblastoma. Humangenetik (1970) 1.05

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22. Am J Hum Genet (1990) 1.04

Loss of 3p or 11p alleles is associated with testicular cancer tumors. Genomics (1989) 1.01

High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods). Hum Genet (1982) 0.97

Multifocal meningiomas in a patient with a constitutional ring chromosome 22. J Med Genet (1986) 0.96

[A case of ring chromosome E 17: 46, XX, r(17) (p13 yields q25) (author's transl)]. Jinrui Idengaku Zasshi (1974) 0.95

Formation of a minichromosome by excision of the proximal region of 17q in a patient with von Recklinghausen neurofibromatosis. Cytogenet Cell Genet (1990) 0.95

Ring chromosome 17 in a mentally retarded boy. Ann Genet (1979) 0.92

Cytogenetic findings on eight follicular thyroid adenomas including one with a t(10;19). Cancer Genet Cytogenet (1989) 0.90

Familial papillary carcinoma of the thyroid. Arch Surg (1981) 0.88

Ring chromosome 4. J Med Genet (1977) 0.88

Model hereditary cancers of man. Prog Nucleic Acid Res Mol Biol (1983) 0.85

Two cases of ring chromosome 11. J Med Genet (1983) 0.84

Constitutional karyotypes in retinoblastoma. Ophthalmic Paediatr Genet (1987) 0.83

A translocation (7;10)(q35;q21) in a differentiated papillary carcinoma of the thyroid. Cancer Genet Cytogenet (1989) 0.81

Two further cases of t(2;13) in alveolar rhabdomyosarcoma indicating a review of the published chromosome breakpoints. Br J Cancer (1987) 0.80

Neurofibromatosis in a man with a ring 22: in situ hybridization studies. Cancer Genet Cytogenet (1987) 0.79

[Retinoblastoma: first case with a ring chromosome 13 in black Africa]. Rev Int Trach Pathol Ocul Trop Subtrop Sante Publique (1987) 0.77

Two forms of ring 13 in a child with rhabdomyosarcoma. Am J Med Genet (1991) 0.77

[Embryonic sarcoma and ring D chromosome]. Ann Genet (1970) 0.77

Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders. J Med Genet (1993) 1.37

Second non-germ cell malignancies after radiotherapy of testicular cancer with or without chemotherapy. Br J Cancer (1990) 1.04

Sporadic gastric carcinomas with microsatellite instability display a particular clinicopathologic profile. Int J Cancer (1995) 0.96

No alterations in exon 21 of the RB1 gene in sarcomas and carcinomas of the breast, colon, and lung. Genes Chromosomes Cancer (1992) 0.80

The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP. Hum Genet (1987) 0.79

[The polyposis project]. Nord Med (1989) 0.78

P53 expression is associated with a high-degree of tumor DNA aneuploidy and incidence of p53 gene mutation, and is localized to the aneuploid component in colorectal carcinomas. Int J Oncol (1993) 0.77

Altered dosage of the sex chromosomes in human testicular cancer: a molecular genetic study. Int J Cancer (1991) 0.75

Chromosome 13 alterations in osteosarcoma cell lines derived from a patient with previous retinoblastoma. Cancer Genet Cytogenet (1991) 0.75

[The polyposis project]. Tidsskr Nor Laegeforen (1988) 0.75