Found: 17
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Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 3, p. 274, doi. 10.1002/gcc.22027
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- Publication type:
- Article
Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 10, p. 2058, doi. 10.1093/hmg/ddr090
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- Publication type:
- Article
Heterozygous TGFBR2 mutations in Marfan syndrome.
- Published in:
- Nature Genetics, 2004, v. 36, n. 8, p. 855, doi. 10.1038/ng1392
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- Publication type:
- Article
Dispermic origin of XY hydatidiform moles.
- Published in:
- Nature, 1981, v. 292, n. 5823, p. 551, doi. 10.1038/292551a0
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- Publication type:
- Article
Prenatal diagnosis of infantile hypophosphatasia.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Chromosome abnormalities in lymph node cells from patient with familial lymphoma. Loss of No. 3 chromosome and presence of large submetacentric chromosome in reticulum cell sarcoma tissue.
- Published in:
- 1968
- By:
- Publication type:
- journal article
Ontogenic studies on the appearance of two classes of immunoglobulin-forming cells in the spleen of the Aleutian skate, Bathyraja aleutica, a cartilaginous fish.
- Published in:
- European Journal of Immunology, 1985, v. 15, n. 9, p. 952, doi. 10.1002/eji.1830150916
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- Publication type:
- Article
Androgenetic origin of hydatidiform mole.
- Published in:
- Nature, 1977, v. 268, n. 5621, p. 633, doi. 10.1038/268633a0
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- Publication type:
- Article
Interstitial deletion of 8p: report of two patients and review of the literature.
- Published in:
- Clinical Genetics, 1995, v. 48, n. 1, p. 41, doi. 10.1111/j.1399-0004.1995.tb04052.x
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- Publication type:
- Article
Occipital horn syndrome: report of a patient and review of the literature.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 1, p. 32, doi. 10.1111/j.1399-0004.1994.tb03986.x
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- Publication type:
- Article
Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence.
- Published in:
- Clinical Genetics, 1993, v. 44, n. 4, p. 169, doi. 10.1111/j.1399-0004.1993.tb03873.x
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- Publication type:
- Article
Y-derived sequence detected in minute chromosomes by polymerase chain reaction and in situ hybridization.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 2, p. 80, doi. 10.1111/j.1399-0004.1992.tb03144.x
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- Publication type:
- Article
Chromosomal aberrations in Sotos syndrome.
- Published in:
- Clinical Genetics, 1992, v. 41, n. 6, p. 335, doi. 10.1111/j.1399-0004.1992.tb03409.x
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- Publication type:
- Article
High resolution-banded chromosomes from patients with Sotos syndrome.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 4, p. 313, doi. 10.1111/j.1399-0004.1991.tb03034.x
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- Publication type:
- Article
Impaired Neutrophil Adhesion: A New Patient in a Previously Reported Family.
- Published in:
- Pediatrics International, 1985, v. 27, n. 4, p. 527, doi. 10.1111/j.1442-200X.1985.tb00675.x
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- Publication type:
- Article
A Weaver-like syndrome in a Japanese boy.
- Published in:
- Clinical Genetics, 1984, v. 25, n. 1, p. 73, doi. 10.1111/j.1399-0004.1984.tb00466.x
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- Publication type:
- Article
Double heteroploidy, 46, XY, t(13q14q), +18, in a spontaneous abortus.
- Published in:
- Clinical Genetics, 1973, v. 4, n. 2, p. 101, doi. 10.1111/j.1399-0004.1973.tb01129.x
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- Publication type:
- Article