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X
Geán, Esther
27  Ergebnisse:
Personensuche X
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1

Molecular characterization of Spanish patients with MECP2 d..:

Pascual‐Alonso, Ainhoa ; Blasco, Laura ; Vidal, Silvia...
Clinical Genetics.  97 (2020)  4 - p. 610-620 , 2020
Link: https://doi.org/10.1111/..
 
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2

Front Cover:

Pascual‐Alonso, Ainhoa ; Blasco, Laura ; Vidal, Silvia...
Clinical Genetics.  97 (2020)  4 - p. , 2020
Link: https://doi.org/10.1111/..
 
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3

An exploratory study of predisposing genetic factors for Di..:

Vergés, Laia ; Vidal, Francesca ; Geán, Esther...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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4

Deletions and duplications of the 22q11.2 region in spermat..:

Vergés, Laia ; Molina, Òscar ; Geán, Esther..
Molecular Cytogenetics.  7 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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5

The ciliary Evc/Evc2 complex interacts with Smo and control..:

Caparrós-Martín, Jose A. ; Valencia, María ; Reytor, Edel...
Human Molecular Genetics.  22 (2012)  1 - p. 124-139 , 2012
Link: https://doi.org/10.1093/..
 
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6

Adults with Sotos syndrome: Review of 21 adults with molecu..:

Fickie, Matthew R. ; Lapunzina, Pablo ; Gentile, Jennifer K....
American Journal of Medical Genetics Part A.  155 (2011)  9 - p. 2105-2111 , 2011
Link: https://doi.org/10.1002/..
 
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7

Macrocephaly–capillary malformation: Analysis of 13 patient..:

Martínez‐Glez, Víctor ; Romanelli, Valeria ; Mori, María A....
American Journal of Medical Genetics Part A.  152A (2010)  12 - p. 3101-3106 , 2010
Link: https://doi.org/10.1002/..
 
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8

Axenfeld–Rieger ocular anomaly and retinoblastoma caused by..:

Roche, Ana ; Mora, Jaume ; Perez, Maria del Mar...
Pediatric Blood & Cancer.  54 (2009)  3 - p. 480-482 , 2009
Link: https://doi.org/10.1002/..
 
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9

Van der Woude Syndrome and Lower Lip Pits Treatment:

Krauel, Lucas ; Parri, Francisco Jose ; Muñoz, Elena...
Journal of Oral and Maxillofacial Surgery.  66 (2008)  3 - p. 589-592 , 2008
Link: https://doi.org/10.1016/..
 
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10

White matter alterations associated with chromosomal disord..:

García‐Cazorla, Angels ; Sans, Anna ; Baquero, Miguel...
Developmental Medicine & Child Neurology.  46 (2004)  3 - p. 148-153 , 2004
Link: https://doi.org/10.1111/..
 
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11

White matter alterations associated with chromosomal disord..:

García-Cazorla, Angels ; Sans, Anna ; Baquero, Miguel...
Developmental Medicine & Child Neurology.  46 (2004)  3 - p. , 2004
Link: https://doi.org/10.1017/..
 
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12

Classic rett syndrome in a boy as a result of somatic mosai..:

Armstrong, Judith ; Póo, Pilar ; Pineda, Mercè...
Annals of Neurology.  50 (2001)  5 - p. 692-692 , 2001
Link: https://doi.org/10.1002/..
 
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13

Identification of a novel rhodopsin mutation (Met-44-Thr) i..:

Reig, Carlos ; Antich, Jaume ; Gean, Esther...
Human Genetics.  94 (1994)  3 - p. , 1994
Link: https://doi.org/10.1007/..
 
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14

Seudoacondroplasia: descripción de un caso de novo y otro f..:

Casas-Alba, Dídac ; Fernández López, Anna ; Gean Molins, Esther..
Anales de Pediatría.  89 (2018)  1 - p. 60-61 , 2018
Link: https://doi.org/10.1016/..
 
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15

Pseudoachondroplasia: Descriptions of a de novo and familia..:

Casas-Alba, Dídac ; Fernández López, Anna ; Gean Molins, Esther..
Anales de Pediatría (English Edition).  89 (2018)  1 - p. 60-61 , 2018
Link: https://doi.org/10.1016/..
 
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