Use of trisomy in Sentences. 25 Examples
The examples include trisomy at the start of sentence, trisomy at the end of sentence and trisomy in the middle of sentence
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trisomy at the start of sentence
- Trisomy has been the focus of extensive medical research but the exact mechanism is still not understood.
trisomy in the middle of sentence
- If this is a patient with trisomy 21, it become more complicated.
- A short femur is associated with trisomy 21 rather than trisomy 13 and holoprosencephaly.
- A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.
- Down syndrome (trisomy 21) is a disorder caused by the presence of an extra 21st chromosome.
- Derivation of a formula for determination of proportion of paternal trisomy 21 is presented.
- Down's syndrome or trisomy 21 occurs in around 1 in 800 births and older women are at higher risk.
- Cases of trisomy 22 usually present with many severe malformations, and they rarely survive to term.
- Fetuses aneuploidies , including trisomy 13 and 18 and triploidy, may have smaller placentas . 9–11.
- A case of partial trisomy 13 is found on a male baby aged 3 months with multiple congenital abnormalities.
- This confirmed the presence of tetrasomy 8 and trisomy 8 and also revealed a low percentage of a pentasomy 8 clone.
- The abnormal is concerned in trisomy, monosomy, Robertsonian translocation, reciprocal translocation and rearrange.
- The nasal bone was absent in 43 of 59 (73%) trisomy 21 fetuses and in three of 603 (0.5%) fetuses with normal karyotype.
- Our findings also point to the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy 21.
- One of their main findings is the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy 21.
- Cases of 18 trisomy, 21 trisomy and Klinefelter Syndrome were diagnosed respectively using the established technique in our lab.
- Polysomy , which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell.
- Relative to fetuses with a nasal bone, those without a nasal bone were estimated to have about 150-times the risk of having trisomy 21.
- Materials and Methods:Cerebral CT findings in 23 cases with 21 trisomy syndrome, proved by cytogenetics, were retrospectively analyzed.
- Conclusion trisomy 16 mice occur with congenital megacolon, and trisomy 16 mice may be also regard as an animal model for Hirschsprung's disease.
- Polysomy, which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell. See nondisjunction.
- Object:To evaluate the prognostic impact of trisomy 8 on cytobiological and clinical features in acute myelomonocytic and monocytic leukemia (M4, M5).
- There is a weak but fairly convincing association between chromosomal abnormalities such as trisomy 21 (Down syndrome) and echogenic foci in the heart.
- Results:(1) 80 cases in 1118 pregnant women were screened as high risk for Down's syndrome, and 1 was verified as trisomy 21 through prenatal diagnosis.
- Objective To explore the value of interphase fluorescence in situ hybridization(I-FISH) on the detection of trisomy 8 in chronic myeloid leukemia(CML) and the progression of CML.
