Search details
1.
Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.
Am J Hum Genet
; 111(3): 487-508, 2024 Mar 07.
Article
in English
| MEDLINE | ID: mdl-38325380
2.
Novel biallelic ZNF335 variant causing primary microcephaly: A case report and radiological review.
Am J Med Genet A
; : e63593, 2024 Mar 28.
Article
in English
| MEDLINE | ID: mdl-38549403
3.
Moral distress in genetic counseling: A study of North American genetic counselors.
J Genet Couns
; 31(4): 836-846, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35044713
4.
Expanding the KIF4A-associated phenotype.
Am J Med Genet A
; 185(12): 3728-3739, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34346154
5.
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype.
J Mol Med (Berl)
; 99(12): 1755-1768, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34536092
6.
Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype.
J Mol Med (Berl)
; 99(12): 1769-1770, 2021 Dec.
Article
in English
| MEDLINE | ID: mdl-34661688
Results
1 -
6
de 6
1
Next >
>>