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Cytogenetic evaluation of 20 primary breast carcinomas
(1997-11-03)
Chromosome analysis was performed on samples from 20 Brazilian patients with breast cancer. All the samples were from untreated patients who presented the clinical symptoms for months or years before surgical intervention. ...
Cytogenetic evaluation of 20 primary breast carcinomas
(1997-11-03)
Chromosome analysis was performed on samples from 20 Brazilian patients with breast cancer. All the samples were from untreated patients who presented the clinical symptoms for months or years before surgical intervention. ...
PARTIAL DELETIONS OF CHROMOSOME-20 AND CHROMOSOME-21 IN A BOY WITH MULTIPLE ANOMALIES AND NORMAL GROWTH-HORMONE (GH) SECRETION
(Univ Chicago Press, 1991-10-01)
PARTIAL DELETIONS OF CHROMOSOME-20 AND CHROMOSOME-21 IN A BOY WITH MULTIPLE ANOMALIES AND NORMAL GROWTH-HORMONE (GH) SECRETION
(Univ Chicago Press, 1991-10-01)
Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies
(2015-12-01)
Terminal deletion in the short arm of chromosome 1 results in a disorder described as 1p36 deletion syndrome. The resulting phenotype varies among patients including mental retardation, developmental delay, sensorineural ...
Low frequency of Y anomaly detected in Australian Brahman cow-herds
(Elsevier B. V., 2015)
Indicine cattle have lower reproductive performance in comparison to taurine. A chromosomal anomaly characterized by the presence Y markers in females was reported and associated with infertility in cattle. The aim of this ...
Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies
(Sociedad Brasileira de Pediatria with Elsevier, 2015)
Objectives
Clinical use of microarray-based techniques for the analysis of many developmental disorders has emerged during the last decade. Thus, chromosomal microarray has been positioned as a first-tier test. This ...
Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies
(Sociedad Brasileira de Pediatria with Elsevier, 2015)
Objectives
Clinical use of microarray-based techniques for the analysis of many developmental disorders has emerged during the last decade. Thus, chromosomal microarray has been positioned as a first-tier test. This ...
Interstitial long-arm deletion of chromosome 7 and ectrodactyly
(1989-01-01)
An interstitial deletion of 7q21 was found in a boy with mental retardation, microcephaly, convergent strabismus, micrognathia, genital anomalies, and other findings, including ectrodactyly.