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Trisomy X and 1 29 translocation in infertile heifers
(1987-12-01)
In a group of 12 Pitangueiras breed heifers exhibiting a high return rate to service, three were noted to be carriers of the 1 29 translocation. One of the heifers exhibited trisomy for the X-chromosome in addition to the ...
Trisomy X and 1 29 translocation in infertile heifers
(1987-12-01)
In a group of 12 Pitangueiras breed heifers exhibiting a high return rate to service, three were noted to be carriers of the 1 29 translocation. One of the heifers exhibited trisomy for the X-chromosome in addition to the ...
Trisomy 9: An additional case with unique manifestations
(Wiley, 1992)
We report on an infant with multiple congenital anomalies and mosaic trisomy 9. Clinical findings are presented, and compared with those of the 24 cases previously reported. Some unusual characteristics found in this patient ...
Trisomy 9: An additional case with unique manifestations
(Wiley, 1992)
We report on an infant with multiple congenital anomalies and mosaic trisomy 9. Clinical findings are presented, and compared with those of the 24 cases previously reported. Some unusual characteristics found in this patient ...
A new case of proximal 10q partial trisomy
(BMJ Publishing Group, 1991)
We report on a girl with mild phenotypic abnormalities and duplication of chromosome 10q11----10q22. The similarities to two previously reported cases with an identical chromosomal aberration provide further support for ...
Regional alteration of cholinergic function in central neurons of trisomy 16 mouse fetuses, an animal model of human trisomy 21 (Down syndrome)
(1994)
The trisomy-16 (TS16) mouse is considered to be a model of human trisomy 21 (Down syndrome) because of genetic homology between mouse chromosome 16 and human chromosome 21. We examined cholinergic function of brain and ...
Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report
(Funpec-editora, 2009-01-01)
The phenotype of partial trisomy 9p includes global developmental delay, microcephaly, bulbous nose, downturned oral commissures, malformed ears, hypotonia, and severe cognitive and language disorders. We present a case ...
Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report
(Funpec-editora, 2009-01-01)
The phenotype of partial trisomy 9p includes global developmental delay, microcephaly, bulbous nose, downturned oral commissures, malformed ears, hypotonia, and severe cognitive and language disorders. We present a case ...
Placentae of fetuses with chromosome 16 trisomy: A morphometric analysis of the interchange chorionic villi
(1998)
We have studied chorionic villi from 38 placentae obtained from spontaneous abortions at 7 to 12 weeks of pregnancy. Samples were separated into four groups: (1) early normal (7-9 weeks of pregnancy, normal karyotype); (2) ...