Williams syndrome and chromosome 18.
نویسندگان
چکیده
منابع مشابه
Cytogenetic analysis of 1284 cases of Down syndrome
Among 17786 karyotyres performed in our center,during 18 years (1357-1375),1300(7.3%) cases of chromosome 21 aberration,including 1284(98.77%) of Down syndrome have been detected.1191 of cases (92.76%) born free trisomy 21:61 cases (4.75%) revealed translocation and 32 cases (2.4%) showed mosaic pattern.among the pateints,59 had robertsonian translocation,2 had translocation between chromosome ...
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Oculo-auriculovertebral dysplasia (Goldenhar) is a congenital syndrome. Its phenotype differs from craniofacial anomalies to cardiac, vertebral or central nervous system defects. This syndrome is rare and its etiology is not apparent yet. Pericentric inversion of chromosome 9 is one of the most common structural balanced chromosomal aberrations with its incidences 15% to 25%. Herein we present ...
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Application of Molecular DNA Markers (STRs) in Molecular Diagnosis of Down Syndrome in Iran
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ورودعنوان ژورنال:
- Journal of medical genetics
دوره 29 9 شماره
صفحات -
تاریخ انتشار 1992