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1.
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
Am J Hum Genet
; 110(5): 809-825, 2023 05 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-37075751
2.
HNRNPR Variants that Impair Homeobox Gene Expression Drive Developmental Disorders in Humans.
Am J Hum Genet
; 104(6): 1040-1059, 2019 06 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-31079900
3.
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Genet Med
; 24(10): 2065-2078, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35980381
4.
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Genet Med
; 23(4): 740-750, 2021 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-33239752
5.
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Genet Med
; 23(12): 2467, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34667295
6.
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.
Hum Genet
; 131(1): 145-56, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-21800092
7.
Practice guidelines for communicating a prenatal or postnatal diagnosis of Down syndrome: recommendations of the national society of genetic counselors.
J Genet Couns
; 20(5): 432-41, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21618060
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