Detalles de la búsqueda
1.
[The Reliability and Validity of the Chinese Version of the Experienced Level of Existential Emptiness].
Hu Li Za Zhi
; 68(5): 30-40, 2021 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-34549406
2.
[Nursing Experience With Reconstructing Self-Control Using Rational-Emotive Behavior Therapy on a Patient With Schizophrenia and Obsessive-Compulsive Symptoms].
Hu Li Za Zhi
; 65(5): 112-119, 2018 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-30276779
3.
Next-generation sequencing identifies rare variants associated with Noonan syndrome.
Proc Natl Acad Sci U S A
; 111(31): 11473-8, 2014 Aug 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-25049390
4.
Using a Visible Light-Polymerized Resin to Fabricate an Interim Partial Removable Dental Prosthesis.
J Prosthodont
; 26(2): 164-167, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27259072
5.
Whole-Exome Sequencing Identified Rare Genetic Variants Associated with Undervirilized Genitalia in Taiwanese Pediatric Patients.
Biomedicines
; 11(2)2023 Jan 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-36830778
6.
New Structural and Single Nucleotide Mutations in Type I and Type II Collagens in Taiwanese Children With Type I and Type II Collagenopathies.
Front Genet
; 12: 594285, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34394176
7.
Identification of a delayed leaf greening gene from a mutation of pummelo.
Sci China Life Sci
; 64(7): 1165-1173, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-33009992
8.
Topographic Analysis of the Isthmus in Mesiobuccal and Mesial Roots of First Molars in a South Korean Population.
Sci Rep
; 10(1): 1247, 2020 01 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-31988399
9.
A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing.
J Microbiol Immunol Infect
; 53(1): 99-105, 2020 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-29551298
10.
Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome.
Front Genet
; 9: 110, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29720996
Resultados
1 -
10
de 10
1
Próxima >
>>