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Author/Creator García‐Alix, Alfredo

1. Hyaline fibromatosis syndrome: Clinical update and phenotype–genotype correlations. Issue 12 (17th September 2018)

Authors:
Casas‐Alba, Dídac; Martínez‐Monseny, Antonio; Pino‐Ramírez, Rosa M.; Alsina, Laia; Castejón, Esperanza; Navarro‐Vilarrubí, Sergi; Pérez‐Dueñas, Belén; Serrano, Mercedes; Palau, Francesc; García‐Alix, Alfredo
Journal:
Human mutation
Issue:
Volume 39:Issue 12(2018)
Page Start:
1752
Record Type:
Journal Article
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2. Okur‐Chung neurodevelopmental syndrome in a patient from Spain. Issue 1 (15th November 2019)

Authors:
Martinez‐Monseny, Antonio F.; Casas‐Alba, Dídac; Arjona, César; Bolasell, Mercè; Casano, Paula; Muchart, Jordi; Ramos, Federico; Martorell, Loreto; Palau, Francesc; García‐Alix, Alfredo; Serrano, Mercedes
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 1(2020)
Page Start:
20
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. The phenotypic spectrum of congenital Zika syndrome. Issue 4 (22nd March 2017)

Authors:
del Campo, Miguel; Feitosa, Ian M. L.; Ribeiro, Erlane M.; Horovitz, Dafne D. G.; Pessoa, André L. S.; França, Giovanny V. A.; García‐Alix, Alfredo; Doriqui, Maria J. R.; Wanderley, Hector Y. C.; Sanseverino, Maria V. T.; Neri, João I. C. F.; Pina‐Neto, João M.; Santos, Emerson S.; Verçosa, Islan...
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 4(2017)
Page Start:
841
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗