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Results 1-4 of 4 (Search time: 0.001 seconds).
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Issue Date
Title
Author(s)
Type
Access Type
2013
Síndrome de Hanhart – caso clínico
Rios, H
;
Carnide, C
;
Morais, S
;
Branco, M
;
Mesquita, J
;
Galhano, E
;
Ramos, L
article
2010
Dilated fetal bowel as indication for prenatal diagnosis of cystic fibrosis
Soares, R
;
Neto, P
;
Pereira, N
;
Cunha, C
;
Pinto, C
;
Fonseca, M
;
Ramos, L
;
Galhano, E
article
Sep-2016
Phenotyping GABA transaminase deficiency: a case description and literature review
Louro, P
;
Ramos, L
;
Robalo, C
;
Cancelinha, C
;
Dinis, A
;
Veiga, R
;
Pina, R
;
Rebelo, O
;
Pop, A
;
Diogo, L
;
Salomons, GS
;
Garcia, P
article
2015
Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients
Carreira, IM
;
Ferreira, SI
;
Matoso, E
;
Pires, LM
;
Ferrão, J
;
Jardim, A
;
Mascarenhas, A
;
Pinto, M
;
Lavoura, N
;
Pais, C
;
Paiva, P
;
Simões, L
;
Caramelo, F
;
Ramos, L
;
Venâncio, M
;
Ramos, F
;
Beleza, A
;
Sá, J
;
Saraiva, J
;
Barbosa de Melo, J
article
Discover
Author
2
Galhano, E
1
Barbosa de Melo, J
1
Beleza, A
1
Branco, M
1
Cancelinha, C
1
Caramelo, F
1
Carnide, C
1
Carreira, IM
1
Cunha, C
1
Dinis, A
.
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Subject
2
Anomalias Congénitas Múltiplas
1
4-Aminobutirato Transaminase/defi...
1
4-Aminobutirato Transaminase/gené...
1
Anomalías Craniofaciais
1
Deficiência Intelectual
1
Deformidades Congénitas dos Membros
1
Diagnóstico Prenatal
1
Doenças do Feto
1
Erros Inatos do Metabolismo
1
Fibrose Quística
.
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Date issued
1
2016
1
2015
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2013
1
2010