Results 311 to 320 of about 3,861,183 (367)
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New England Journal of Medicine, 1976
The sex chromosome abnormalities are one of the most common types of chromosome disorders, occurring once among every 1100 females and once among every 380 males.
P. Gerald
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The sex chromosome abnormalities are one of the most common types of chromosome disorders, occurring once among every 1100 females and once among every 380 males.
P. Gerald
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CRC Critical Reviews in Clinical Laboratory Sciences, 1981
A critical and comprehensive review of the major sex chromosome disorders. The introduction briefly outlines the cytogenetic background to these disorders and refers to earlier reviews. The paper then reviews the clinical and psychiatric aspects of the various chromosome disorders.
David Pitcher
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A critical and comprehensive review of the major sex chromosome disorders. The introduction briefly outlines the cytogenetic background to these disorders and refers to earlier reviews. The paper then reviews the clinical and psychiatric aspects of the various chromosome disorders.
David Pitcher
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Chromosome disorders and epilepsy
Clinical Neurophysiology, 2007 S. Macleod +5 more
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Autosomal chromosome disorders and variations.
New England Journal of Medicine, 1976Chromosomal abnormalities or variations are related to genetics in three ways: they involve the genetic material, and in that sense are always "genetic"; most of the variants and a proportion of the structural rearrangements are directly transmitted from parent to offspring (i.e., such changes can be inherited); and some of the chromosome abnormalities
O. J. Miller, W. R. Breg
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Prenatal diagnosis of chromosome disorders.
British Medical Bulletin, 1976K. Laurence, P. Gregory
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Genomic disorders on chromosome 22
Current Opinion in Pediatrics, 2012Chromosome 22, the first human chromosome to be completely sequenced, is prone to genomic alterations. Copy-number variants (CNVs) are common because of an enrichment of low-copy repeat sequences that precipitate a high frequency of nonallelic homologous misalignments and unequal recombination during meiosis.
Shihui Yu, W. Graf, R. Shprintzen
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