How To Use Trisomy In A Sentence
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Trisomy 18 was shown, in an index case, by G-banded karyotyping.
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We conclude that trisomy 18 is a consistent feature in pilomatricoma, suggesting that genes carried on this chromosome, such as that for the antiapoptotic oncoprotein BCL2, may have a role in the growth and differentiation of this benign self-limited tumor.
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Johnson MP, Childs MD, Isada NB, Koppitch III GC, Evans MI: Trisomy 16 CVS and viable pregnancy: Lethal aneuploidy compartmentalized to the trophoblast in two otherwise normal pregnancies.
Prenatal Diagnosis
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Trisomy 21 placentas: Histopathological and immunohistochemical findings using proliferating cell nuclear antigen (PCNA) Fetal Diagnosis and Therapy 12 (4), 210-215, 1997.
Prenatal Diagnosis
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First-trimester trisomy screening: nuchal translucency measurement training and quality assurance to correct and unify technique.
Prenatal Diagnosis
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Both monosomy and trisomy of specific chromosomes are associated with developmental defects and cancer risk.
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It hasn't been called Trisomy G for decades, since the days when the common term for it was "mongolism.
Latest Articles
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Our findings also point to the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy 21.
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Most trisomy fetuses are spontaneously aborted.
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Both monosomy and trisomy of specific chromosomes are associated with developmental defects and cancer risk.
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A common type of chromosomal abnormality is called a trisomy.
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Multiple gestation, gestational trophoblastic disease, triploidy, trisomy 21 syndrome, and hydrops fetalis have been associated with an increased incidence of hyperemesis gravidarum.
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The predominant anomalies in reproductive specimens include trisomy of the autosomes and monosomy of the X chromosome.
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Triple screening should not replace amniocentesis or chorionic villous sampling in pregnancies at high risk for trisomy 21.
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First-trimester screening also can help detect other chromosomal abnormalities such as trisomy 18.
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If the proband has trisomy 21, the likelihood of a trisomy 21 pregnancy is minimally increased for family members other than the parents.
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One of their main findings is the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy 21.
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Down syndrome is sufficient to refute this point, since individuals with trisomy 21 can indeed mate with euploid individuals.
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