Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lilia Maria Azevedo Moreira"'
Publikováno v:
Case Reports in Genetics, Vol 2019 (2019)
Individuals with ring chromosome 13 may show characteristics observed in a deletion syndrome and could present a set of dismorphies along with intellectual disability, according to chromosomal segments involved in the genetic imbalance. Nevertheless,
Externí odkaz:
https://doaj.org/article/1fb14d5398af41cc9708f0e97cb66a48
Autor:
Mariluce Riegel, Nathália Barcellos, Rafaella Mergener, Karen Regina Silva de Souza, Júlio César Loguercio Leite, Rejane Gus, Lilia Maria Azevedo Moreira, Roberto Giugliani
Publikováno v:
Clinical and Biomedical Research, Vol 34, Iss 4 (2014)
Introduction: During the past few decades, the number of diseases identified to be caused by chromosomal microdeletions has increased quickly, bringing a new and crucial role for cytogenetics on the diagnosis of these conditions. The purpose of this
Externí odkaz:
https://doaj.org/article/9722cfa8ac53483281a24f66cac910e3
Publikováno v:
CYTOLOGIA. 44:21-27
Chromosomes of M. quadrifasciata anthidioides pupae, obtained by squash preparations from ovaries, were analysed through proteolitic digestion with trypsine and subsequent staining with Giemsa. The G-bands were described according to the nomenclature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e43493d6328e8d1710a40308f853b69
https://doi.org/10.1508/cytologia.44.21
https://doi.org/10.1508/cytologia.44.21
Publikováno v:
Arquivos de Neuro-Psiquiatria v.34 n.4 1976
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 34, Issue: 4, Pages: 374-378, Published: DEC 1976
Arquivos de Neuro-Psiquiatria, Vol 34, Iss 4, Pp 374-378 (1976)
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 34, Issue: 4, Pages: 374-378, Published: DEC 1976
Arquivos de Neuro-Psiquiatria, Vol 34, Iss 4, Pp 374-378 (1976)
Os autores registram um caso de retardo neuromotor em paciente com cromossomo 1qh+. A análise cromossômica do paciente e três familiares revelou igualmente em todos, aumento do braço longo do cromossomo n.° 1. Entretanto, é considerada a possib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd910fb0b37193b8c2d2815e45e71a2a
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1976000400008
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1976000400008
