CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROME
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference7 articles.
1. RISK OF PARENTS WHO HAVE HAD ONE CHILD WITH DOWN'S SYNDROME (MONGOLISM) HAVING ANOTHER CHILD SIMILARLY AFFECTED
2. CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISM
3. 21-TRISOMY/NORMAL MOSAICISM
4. CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILD
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2. Prevention and Periodontal Treatment in Down Syndrome Patients: A Systematic Review;PLOS ONE;2016-06-29
3. Assessment of cardiac function in absence of congenital and acquired heart disease in patients with Down syndrome;World Journal of Pediatrics;2016-04-08
4. Identification by fluorescence of apparently extra human F chromosomes as G chromosomes with giant satellites;Hereditas;2009-02-12
5. RECENT ADVANCES IN DOWN'S ANOMALY (MONGOLISM);Developmental Medicine & Child Neurology;2008-11-12
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