Un alumne de Medicina de la UIB publica un estudi sobre la síndrome de les ungles grogues en una revista científica - Hemeroteca - Diari de la UIB - Universitat de les Illes Balears
The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype–phenotype correlations | Genetics in Medicine
La sindrome di Bosch (Italian Edition): Bassoli, Roberto: 9788831398299: Amazon.com: Books
Un alumno de la UIB participa en un estudio sobre el síndrome de uñas amarillas
Síndrome de atrofia óptica de Bosch-Boonstra-Schaaf
La sindrome di Bosch" la nuova opera di Roberto Bassoli
Bosch-Boonstra-Schaaf optic atrophy syndrome mimicking septo-optic dysplasia in a 10-year-old child - ScienceDirect
Special Needs Spotlight || Colton » This Little Miggyz
Novel dominant-negative NR2F1 frameshift mutation and a phenotypic expansion of the Bosch-Boonstra-Schaaf optic atrophy syndrome - ScienceDirect
Mariana de Ugarte: «Ante el síndrome de Down hay que superar los miedos»
Sidelle :: BOSCH-BOONSTRA SCHAAF OPTIC ASTROPHY SYNDROME » SWEET NECTAR SOCIETY
An inaugural family conference for Bosch-Boonstra-Schaaf Optic Atrophy Syndrome brings together key stakeholders | NRI
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Bosch-Boonstra-Schaaf optic atrophy syndrome mimicking septo-optic dysplasia in a 10-year-old child - ScienceDirect
Sidelle :: BOSCH-BOONSTRA SCHAAF OPTIC ASTROPHY SYNDROME » SWEET NECTAR SOCIETY
Modelo experimental para un tipo de atrofia humana del nervio óptico
NR2F1 Foundation - For those with rare NR2F1 gene mutation
NR2F1 Foundation - Countdown to Rare Disease Day with the ABC's of NR2F1! B is for BBSOAS, Bosch Boonstra Schaaf optic atrophy syndrome #NR2F1Foundation #NR2F1 #BBSOAS #careaboutrare #RareDiseaseDay2021 #genetics | Facebook
LA SINDROME D STENDHAL | JAUME BOSCH | Casa del Libro
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome & Hypotonia
10.ES Síndrome de dilatación-torsión de estómago. (Dr. Luis Bosch) - YouTube
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome & Epilepsy
Síndrome de Van der Bosch – FEMEXER
A severe case of Bosch–Boonstra–Schaaf optic atrophy syndrome with a novel description of coloboma and septo‐optic dysplasia, owing to a start codon variant in the NR2F1 gene - Gazdagh - 2022 -
