Browse by Publication

Up a level
Export as [feed] Atom [feed] RSS
Group by: Year | Authors/Creators | Item Type | Full Text
Jump to: 2018 | 2017 | 2015 | 2013 | 2012
Number of items: 10.

2018

Blencowe, H; Moorthie, S; Darlison, MW; Gibbons, S; Modell, B; Congenital Disorders Expert Group; , COLLABORATORS; Bittles, AH; Blencowe, H; Christianson, A; +19 more... Cousens, S; Darlison, M; Gibbons, S; Hamamy, H; Khoshnood, B; Howson, CP; Lawn, JE; Mastroiacovo, P; Modell, B; Moorthie, S; Morris, JK; Mossey, PA; Neville, AJ; Petrou, M; Povey, S; Rankin, J; Schuler-Faccini, L; Wren, C; Yunis, KA; (2018) Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders. Journal of community genetics. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-018-0359-3
[img]

Blencowe, H; Moorthie, S; Petrou, M; Hamamy, H; Povey, S; Bittles, A; Gibbons, S; Darlison, M; Modell, B; Congenital Disorders Expert Group; +23 more... , COLLABORATORS; Bittles, AH; Blencowe, H; Christianson, A; Cousens, S; Darlison, M; Gibbons, S; Hamamy, H; Khoshnood, B; Howson, CP; Lawn, JE; Mastroiacovo, P; Modell, B; Moorthie, S; Morris, JK; Mossey, PA; Neville, AJ; Petrou, M; Povey, S; Rankin, J; Schuler-Faccini, L; Wren, C; Yunis, KA; (2018) Rare single gene disorders: estimating baseline prevalence and outcomes worldwide. Journal of community genetics. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-018-0376-2
[img]

Modell, B; Darlison, MW; Malherbe, H; Moorthie, S; Blencowe, H; Mahaini, R; El-Adawy, M; (2018) Congenital disorders: epidemiological methods for answering calls for action. Journal of community genetics. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-018-0390-4 Full text not available from this repository.

Moorthie, S; Blencowe, H; Darlison, MW; Lawn, J; Morris, JK; Modell, B; Congenital Disorders Expert Group; Bittles, AH; Blencowe, H; Christianson, A; +19 more... Cousens, S; Darlison, MW; Gibbons, S; Hamamy, H; Khoshnood, B; Howson, CP; Lawn, J; Mastroiacovo, P; Modell, B; Moorthie, S; Morris, JK; Mossey, PA; Neville, AJ; Petrou, M; Povey, S; Rankin, J; Schuler-Faccini, L; Wren, C; Yunnis, KA; (2018) Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide. Journal of community genetics. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-018-0384-2
[img]

2017

Moorthie, S; Blencowe, H; Darlison, MW; Gibbons, S; Lawn, JE; Mastroiacovo, P; Morris, JK; Modell, B; Congenital Disorders Expert Group; , COLLABORATORS; +22 more... Bittles, AH; Blencowe, H; Christianson, A; Cousens, S; Darlison, MW; Gibbons, S; Hamamy, H; Khoshnood, B; Howson, CP; Lawn, JE; Mastroiacovo, P; Modell, B; Moorthie, S; Morris, JK; Mossey, PA; Neville, AJ; Petrou, M; Povey, S; Rankin, J; Schuler-Faccini, L; Wren, C; Yunis, KA; (2017) Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide. Journal of community genetics. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-017-0336-2
[img]

Moorthie, S; Blencowe, H; W Darlison, M; Lawn, JE; Mastroiacovo, P; Morris, JK; Modell, B; Congenital Disorders Expert Group; , COLLABORATORS; Bittles, AH; +21 more... Blencowe, H; Christianson, A; Cousens, S; Darlison, MW; Gibbons, S; Hamamy, H; Khoshnood, B; Howson, CP; Lawn, JE; Mastroiacovo, P; Modell, B; Moorthie, S; Morris, JK; Mossey, PA; Neville, AJ; Petrou, M; Povey, S; Rankin, J; Schuler-Faccini, L; Wren, C; Yunis, KA; (2017) An overview of concepts and approaches used in estimating the burden of congenital disorders globally. Journal of community genetics. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-017-0335-3
[img]

2015

Larrandaburu, M; Matte, U; Noble, A; Olivera, Z; Sanseverino, MT; Nacul, L; Schuler-Faccini, L; (2015) Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm. Journal of community genetics, 6 (3). pp. 241-9. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-015-0236-2 Full text not available from this repository.

2013

Schuler-Faccini, L; Sanseverino, MT; de Rocha Azevedo, LM; Moorthie, S; Alberg, C; Chowdhury, S; Sagoo, GS; Burton, H; Nacul, LC; (2013) Health needs assessment for congenital anomalies in middle-income countries: Examining the case for neural tube defects in Brazil. Journal of community genetics, 5 (2). pp. 147-55. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-013-0165-x Full text not available from this repository.

2012

Groisman, B; Liascovich, R; Barbero, P; Alberg, C; Moorthie, S; Nacul, L; Sagoo, GS; (2012) The use of a Toolkit for health needs assessment on neural tube defects in Argentina. Journal of community genetics, 4 (1). pp. 77-86. ISSN 1868-310X DOI: https://doi.org/10.1007/s12687-012-0120-2 Full text not available from this repository.

This list was generated on Tue Nov 13 17:40:38 2018 GMT.