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Viguetti-Campos, Nilma Lucia
15  results:
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1

Clinical and laboratory differences between chromosomal and..:

Riccetto, Luísa ; Vieira, Tarsis Paiva ; Viguetti-Campos, Nilma Lucia...
Sao Paulo Medical Journal.  141 (2023)  4 - p. , 2023
Link: https://doi.org/10.1590/..
 
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2

Further evidence for lack of association of PRDM9 polymorph..:

Carvalho, Pedro Cristovão ; Sgardioli, Ilária Cristina ; Bonadia, Luciana Cardoso...
Meta Gene.  29 (2021)  - p. 100927 , 2021
Link: https://doi.org/10.1016/..
 
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3

408 Cases of Genital Ambiguity Followed by Single Multidisc..:

De Paula, Georgette Beatriz ; Barros, Beatriz Amstalden ; Carpini, Stela...
International Journal of Endocrinology.  2016 (2016)  - p. 1-9 , 2016
Link: https://doi.org/10.1155/..
 
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4

Local Strategies to Address Health Needs of Individuals wit..:

Fontes, Marshall Ítalo Barros ; Almeida, Lanusia Nunes ; De Oliveira Reis Junior, Gilberto...
The Cleft Palate-Craniofacial Journal.  50 (2013)  4 - p. 424-431 , 2013
Link: https://doi.org/10.1597/..
 
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5

A new case of partial 14q31.3-qter trisomy due to maternal ..:

Sgardioli, Ilária Cristina ; Simioni, Milena ; Viguetti-Campos, Nilma Lúcia..
Gene.  523 (2013)  2 - p. 192-194 , 2013
Link: https://doi.org/10.1016/..
 
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6

Rare 15q21.1q22.31 Duplication Due to a Familial Chromosoma..:

Nascimento, Carolina Gama ; Prota, Joana Rosa Marques ; Sgardioli, Ilária Cristina...
Genes.  14 (2023)  4 - p. 885 , 2023
Link: https://doi.org/10.3390/..
 
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7

SOX3 duplication in a boy with 46,XX ovotesticular disorder..:

de Oliveira, Flávia Marcorin ; Barros, Beatriz Amstalden ; dos Santos, Ana Paula...
American Journal of Medical Genetics Part A.  191 (2022)  2 - p. 592-598 , 2022
Link: https://doi.org/10.1002/..
 
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8

Alterações cromossômicas nas síndromes de Prader-Willi e An..:

Nascimento, Flavia Caroline ; Rezende, Lúciana Montes ; Santos, Ana Paula dos...
https://ojs.uel.br/revistas/uel/index.php/seminabio/article/view/29385/22489.  , 2018
Link: https://ojs.uel.br/revis..
 
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9

Rare 15q21.1q22.31 Duplication Due to a Familial Chromosoma..:

Carolina Gama Nascimento ; Joana Rosa Marques Prota ; Ilária Cristina Sgardioli...
https://www.mdpi.com/2073-4425/14/4/885.  , 2023
Link: https://doi.org/10.3390/..
 
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10

Rare 15q21.1q22.31 Duplication Due to a Familial Chromosoma..:

Carolina Gama Nascimento ; Joana Rosa Marques Prota ; Ilária Cristina Sgardioli...
Cytogenomics.  , 2023
Link: https://doi.org/10.3390/..
 
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11

Clinical and laboratory differences between chromosomal and..:

Luísa Riccetto ; Tarsis Paiva Vieira ; Nilma Lucia Viguetti-Campos...
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802022005029201&tlng=en.  , 2022
Link: https://doi.org/10.1590/..
 
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12

408 Cases of Genital Ambiguity Followed by Single Multidisc..:

Georgette Beatriz De Paula ; Beatriz Amstalden Barros ; Stela Carpini...
http://dx.doi.org/10.1155/2016/4963574.  , 2016
Link: https://doi.org/10.1155/..
 
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13

Why pediatricians need to know the disorders of sex develop..:

Beck, Mayra de Souza El ; Germano, Carlos W. ; Barros, Beatriz A....
Jornal de Pediatria.  96 (2020)  5 - p. 607-613 , 2020
Link: https://doi.org/10.1016/..
 
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14

Identification of a neocentromere in a rearranged Y chromos..:

Godoy Assumpção, Juliana ; Berkofsky‐Fessler, Windy ; Viguetti Campos, Nilma...
American Journal of Medical Genetics.  113 (2002)  3 - p. 263-267 , 2002
Link: https://doi.org/10.1002/..
 
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15

Cranio-oculo-fronto-nasal malformation: a new MCA condition:

GIL DA SILVA LOPES, VERA L??CIA ; VIGUETTI CAMPOS, NILMA L??CIA ; MACIEL-CUERRA, ANDR??EA TREVAS
Clinical Dysmorphology.  6 (1997)  1 - p. 25???30 , 1997
Link: https://doi.org/10.1097/..
 
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