Search details
1.
Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C.
Prenat Diagn
; 44(3): 369-372, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38163266
2.
RASopathies: A significant cause of polyhydramnios?
Prenat Diagn
; 41(3): 362-367, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33150592
3.
Prenatal treatment of ornithine transcarbamylase deficiency.
Mol Genet Metab
; 123(3): 297-300, 2018 03.
Article
in English
| MEDLINE | ID: mdl-29396029
4.
Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal Period.
J Ultrasound Med
; 35(6): 1353-8, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-27162279
5.
46,XY disorders of sex development and congenital diaphragmatic hernia: a case with dysmorphic facies, truncus arteriosus, bifid thymus, gut malrotation, rhizomelia, and adactyly.
Am J Med Genet A
; 167(6): 1360-4, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25898814
6.
Clinical whole-exome sequencing: are we there yet?
Genet Med
; 16(9): 717-9, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24525916
7.
Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome.
Am J Med Genet A
; 164A(11): 2814-21, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-25250515
8.
Prenatally diagnosed omphalocele: characteristics associated with adverse neonatal outcomes.
J Perinatol
; 39(8): 1111-1117, 2019 Aug.
Article
in English
| MEDLINE | ID: mdl-31227786
Results
1 -
8
de 8
1
Next >
>>