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1 Objective:A few trisomy 21 cells in normal chromosome karyotype was been observed for study of the correlation of clinical phenotype and development damage in sick children of Down's syndrome.

2 Fetuses aneuploidies , including trisomy 13 and 18 and triploidy, may have smaller placentas . 9–11.

3 Down syndrome (trisomy 21) is a disorder caused by the presence of an extra 21st chromosome.

4 A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

5 Object:To evaluate the prognostic impact of trisomy 8 on cytobiological and clinical features in acute myelomonocytic and monocytic leukemia (M4, M5).

6 A short femur is associated with trisomy 21 rather than trisomy 13 and holoprosencephaly.

7 This confirmed the presence of tetrasomy 8 and trisomy 8 and also revealed a low percentage of a pentasomy 8 clone.

8 Synchronous firing trisomy has been used many calligraphy lovers, yes there is scientific in nature,(www.Sentencedict.com) are totally beginner can practice calligraphy calligraphy are used via.

9 The abnormal is concerned in trisomy, monosomy, Robertsonian translocation, reciprocal translocation and rearrange.

10 Trisomy has been the focus of extensive medical research but the exact mechanism is still not understood.

11 Polysomy , which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell.

12 If this is a patient with trisomy 21, it become more complicated.

13 Cases of 18 trisomy, 21 trisomy and Klinefelter Syndrome were diagnosed respectively using the established technique in our lab.

14 Cases of trisomy 22 usually present with many severe malformations, and they rarely survive to term.

15 Conclusion Trisomy 16 mice occur with congenital megacolon, and trisomy 16 mice may be also regard as an animal model for Hirschsprung's disease.

16 Down's syndrome or trisomy 21 occurs in around 1 in 800 births and older women are at higher risk.

17 A case of partial trisomy 13 is found on a male baby aged 3 months with multiple congenital abnormalities.

18 Polysomy, which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell. See nondisjunction.

19 Our findings also point to the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy 21.

20 One of their main findings is the increasing importance of fetal ultrasonography in the prenatal diagnosis of fetal trisomy 21.

21 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.

22 There is a weak but fairly convincing association between chromosomal abnormalities such as trisomy 21 (Down syndrome) and echogenic foci in the heart.

23 Materials and Methods:Cerebral CT findings in 23 cases with 21 trisomy syndrome, proved by cytogenetics, were retrospectively analyzed.

24 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.

25 Derivation of a formula for determination of proportion of paternal trisomy 21 is presented.

26 The nasal bone was absent in 43 of 59 (73%) trisomy 21 fetuses and in three of 603 (0.5%) fetuses with normal karyotype.

27 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.

28 Objective To evaluate significance of prenatal ultrasonography in diagnosis of trisomy 18.