Detalles de la búsqueda
1.
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions.
Am J Hum Genet
; 101(6): 985-994, 2017 Dec 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29198724
2.
Acromicric dysplasia due to a novel missense mutation in the fibrillin 1 gene in a three-generation family.
J Pediatr Endocrinol Metab
; 35(11): 1443-1447, 2022 Nov 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-35942587
Resultados
1 -
2
de 2
1
Próxima >
>>