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pro vyhledávání: '"Néria A. Maia"'
Autor:
Tamara Borgonovo, Enilze M.S.F. Ribeiro, Déborah Afonso Cornélio, Ana Teresa Schmid-Braz, Valderez Ravaglio Jamur, Lismeri Wuicik, Loraine Beatriz Acosta Veiga, Néria A. Maia Ehmke, Ricardo Pasquini, Iglenir João Cavalli
Publikováno v:
Genetics and Molecular Biology, Vol 28, Iss 4, Pp 654-660 (2005)
Bone marrow cytogenetic studies were performed on 93 patients with primary myelodysplastic syndrome (MDS) diagnosed at the Clinical Hospital of the Federal University of Paraná, Brazil. Chromosomal alterations were observed in 69% of the patients. M
Externí odkaz:
https://doaj.org/article/8a2368b4fd204974986c06b7020ca537
Autor:
Déborah Afonso Cornélio, Valderez Ravaglio Jamur, Tamara Borgonovo, Néria A. Maia Ehmke, Loraine Beatriz, Ricardo Pasquini, Lismeri Wuicik, Acosta Veiga, Ana Teresa Schmid-Braz, Iglenir J. Cavalli
Publikováno v:
Genetics and Molecular Biology, Vol 28, Iss 4, Pp 654-660 (2005)
Genetics and Molecular Biology, Volume: 28, Issue: 4, Pages: 654-660, Published: DEC 2005
Genetics and Molecular Biology v.28 n.4 2005
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 28, Issue: 4, Pages: 654-660, Published: DEC 2005
Genetics and Molecular Biology v.28 n.4 2005
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Bone marrow cytogenetic studies were performed on 93 patients with primary myelodysplastic syndrome (MDS) diagnosed at the Clinical Hospital of the Federal University of Paraná, Brazil. Chromosomal alterations were observed in 69% of the patients. M
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Publikováno v:
Human Heredity. 30:225-231
A large Brazilian kindred of German origin with 117 individuals with the A2 (Mohr-Wriedt) bradydactyly is presented. Some drawings based on radiographs and revealing the high phenotypic spectrum of the malformation are presented. Our corrected data s
Autor:
Mary Whittaker, P.R. Rao, Bernardo Erdtmann, C. Rahuel, Rosa Maria Corbo, Yoshiro Wada, R. Palmarino, R.J. Mitchell, Gérard Lucotte, E. Calzolari, K.B. Gopalam, M. Frain, S. Lavareda de Souza, Cécile Rahuel, D.G. Woodfield, Renato Scacchi, José M. Sala-Trepat, F. Martuzzi Veronesi, Luc Noel, G. Marogna, Ives José Sbalqueiro, Judith J. Britten, K. Sampat Narasimha Char, Kusuki Nishoka, G. Mulas, Rick Johnson, G. Cossu, C.R. Srikumari, Hisashi Yamanaka, A. Stangoni, G. Laconi, Davide Pettener, Paola Lucarelli, Néria A. Maia, J. Rajanikumari, S.A. Fabb, Iglenir J. Cavalli, G.B. Cuccuru, Tsutomu Ohtani, C.J. Lyne, Naoyuki Kamatani, P.L. Clark, M.A. Lyne, Michio Kobayashi, Margarete S. Mattevi, T. Venkateswara Rao, Kiyonobu Mikanagi
Publikováno v:
Human Heredity. 35:I-VI
Autor:
Ives José Sbalqueiro, Margarete S. Mattevi, Néria A. Maia, Iglenir J. Cavalli, Bernardo Erdtmann
Publikováno v:
Human Heredity. 34:62-64
A comparative analysis of the C bands of chromosomes 1, 9, 16 and Y of 27 Caucasian and 27 Japanese males is reported. The mean of the total centromeric heterochromatin of the three pairs (sigma h1, 9, 16) is larger in Caucasian than in Japanese subj
Autor:
Elza Costa Netto Muniz, Néria A. Maia, Iglenir J. Cavalli, Lúcia Regina Ribeiro, Euclides Fontoura da Silva Junior, Ives José Sbalqueiro
Publikováno v:
Acta Biológica Paranaense. 17
Citogenética e raça: um estudo em índios Kaingáng do Paraná
Autor:
Néria A. Maia, Iglenir J. Cavalli, Ives José Sbalqueiro, Bernardo Erdtmann, Margarete S. Mattevi
Publikováno v:
Human heredity. 35(6)
A quantitative analysis of C bands by densitometric measurements in chromosomes 1, 9, 16, and Y was conducted in Caucasians and Japanese living in Brazil. Sixty normal unrelated subjects (30 males and 30 females) were studied in each racial group. Ca
Autor:
Néria A. Maia, A. C. de Figueiredo, N. Frejre-Maia, John M. Opitz, J. Felizau, Marisa Parreira
Publikováno v:
Clinical genetics. 10(5)
Hypertrichosis lanuginosa (without gingival hyperplasia) is described in a mother and son; the latter also had photophobia, infantile genitalia, growth retardation, hypotension, low IQ and dental abnormalities (hyperdontia, permanence of deciduous an
Autor:
Mary Whittaker, Margarete S. Mattevi, C.R. Srikumari, Cécile Rahuel, G. Laconi, Rick Johnson, C. Rahuel, Luc Noel, Judith J. Britten, R.J. Mitchell, Tsutomu Ohtani, C.J. Lyne, G. Marogna, Renato Scacchi, E. Calzolari, Paola Lucarelli, Bernardo Erdtmann, G.B. Cuccuru, Ives José Sbalqueiro, Gérard Lucotte, Kiyonobu Mikanagi, S. Lavareda de Souza, M. Frain, R. Palmarino, Néria A. Maia, Iglenir J. Cavalli, D.G. Woodfield, G. Cossu, Yoshiro Wada, G. Mulas, K. Sampat Narasimha Char, Naoyuki Kamatani, Davide Pettener, P.L. Clark, Hisashi Yamanaka, Rosa Maria Corbo, Kusuki Nishoka, J. Rajanikumari, T. Venkateswara Rao, M.A. Lyne, F. Martuzzi Veronesi, José M. Sala-Trepat, A. Stangoni, Michio Kobayashi, S.A. Fabb, P.R. Rao, K.B. Gopalam
Publikováno v:
Human Heredity. 35:408-409