Add to ORKGChromosomal aberrations are one of the most frequent causes of multiple congenital malformations and mental retardation. Trisomy 21, 18 and 13 are the most common varieties of autosomal trisomy recognized at birth; most of the others lead to spontaneous abortions in the first trimester’. Full trisomy 9 is rare in live born infants, but trisomy 9 mosaic ism has been reported and compatible with life. Unlike trisomy 21, 18 and 13, the range of clinical manifestation has not been well described, especially with respect to mental status1,2
Trisomy for the distal third of the long arm of chromosome 19 was observed in a 12-year-old boy and ...
Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 9 Materials...
Background: Non-invasive prenatal testing (NIPT) is currently used as a frontline screening test to ...
suMMARY Two unrelated newborn infants with multiple malformations were found to have complete trisom...
We present a case in which amniocentesis performed at 33 weeks\u27 gestation because of symmetrical ...
Trisomy 9p may occur due to either parental reciprocal translocation of chromosome 9 with other chro...
This communication reports prenatal diagnosis of partial trisomy 21 resulting from balanced transloc...
A new patient with trisomy for the chromosome segment 9pter+q22 is compared to 19 previously reporte...
Aim of the Work: To report a newborn infant with multiple congenital anomalies and apparent complete...
Summary. Six cases of translocation trisomy for the distal half of the short arm of a number 9 chrom...
ABSTRACT A rare case of trisomy 9 p syndrome resulting from maternal reciprocal translocation is rep...
This communication reports prenatal diagnosis of partial trisomy 21 resulting from balanced transloc...
This communication reports prenatal diagnosis of partial trisomy 21 resulting from balanced transloc...
Abstract The most common congenital anomalies, autosomal aneuploidies are linked to a variety of m...
Mosaicism for an extra chromosome 9 was found in an underweight male newborn with multiple malformat...
Trisomy for the distal third of the long arm of chromosome 19 was observed in a 12-year-old boy and ...
Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 9 Materials...
Background: Non-invasive prenatal testing (NIPT) is currently used as a frontline screening test to ...
suMMARY Two unrelated newborn infants with multiple malformations were found to have complete trisom...
We present a case in which amniocentesis performed at 33 weeks\u27 gestation because of symmetrical ...
Trisomy 9p may occur due to either parental reciprocal translocation of chromosome 9 with other chro...
This communication reports prenatal diagnosis of partial trisomy 21 resulting from balanced transloc...
A new patient with trisomy for the chromosome segment 9pter+q22 is compared to 19 previously reporte...
Aim of the Work: To report a newborn infant with multiple congenital anomalies and apparent complete...
Summary. Six cases of translocation trisomy for the distal half of the short arm of a number 9 chrom...
ABSTRACT A rare case of trisomy 9 p syndrome resulting from maternal reciprocal translocation is rep...
This communication reports prenatal diagnosis of partial trisomy 21 resulting from balanced transloc...
This communication reports prenatal diagnosis of partial trisomy 21 resulting from balanced transloc...
Abstract The most common congenital anomalies, autosomal aneuploidies are linked to a variety of m...
Mosaicism for an extra chromosome 9 was found in an underweight male newborn with multiple malformat...
Trisomy for the distal third of the long arm of chromosome 19 was observed in a 12-year-old boy and ...
Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 9 Materials...
Background: Non-invasive prenatal testing (NIPT) is currently used as a frontline screening test to ...