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1.
Investigation of the Relationship Between Religious Attitude and Postpartum Physical and Perineal Pain in Iran.
J Relig Health
; 62(5): 3313-3326, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37460863
2.
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice.
Genome Res
; 26(2): 183-91, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26755636
3.
Targeted next generation sequencing reveals genetic defects underlying inherited retinal disease in Iranian families.
Mol Vis
; 25: 106-117, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30820146
4.
The Relationship Between Body Mass Index (BMI) and Menstrual Disorders at Different Ages of Menarche and Sex Hormones.
J Natl Med Assoc
; 110(5): 440-447, 2018 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-30129516
5.
A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation.
Am J Med Genet A
; 170(3): 615-21, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26581570
6.
Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
Gut
; 63(1): 80-7, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23850713
7.
Association of CETP Taq1B and -629C > A polymorphisms with coronary artery disease and lipid levels in the multi-ethnic Singaporean population.
Lipids Health Dis
; 12: 85, 2013 Jun 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-23758630
8.
Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome.
Ann Clin Transl Neurol
; 10(5): 787-801, 2023 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-37000947
9.
Diagnostic yield of exome sequencing in congenital vertical talus.
Eur J Med Genet
; 65(6): 104514, 2022 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-35487415
10.
Investigation of the role of herbal medicine, acupressure, and acupuncture in the menopausal symptoms: An evidence-based systematic review study.
J Family Med Prim Care
; 9(6): 2638-2649, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32984100
11.
Determining genetic variants in children and adolescents suffering from tetralogy of Fallot with a positive family history: methodology.
Acta Biomed
; 91(4): e2020096, 2020 06 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-33525261
12.
Investigation of correlation between religious attitude and mother-adolescent girls conflict.
J Family Med Prim Care
; 8(9): 2893-2897, 2019 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-31681662
13.
The effect of aromatherapy on mental, physical symptoms, and social functions of females with premenstrual syndrome: A randomized clinical trial.
J Family Med Prim Care
; 8(9): 2990-2996, 2019 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-31681680
14.
Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.
Stem Cell Reports
; 13(6): 1126-1141, 2019 12 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31813827
15.
Cornelia de lange syndrome.
Indian J Hum Genet
; 14(1): 23-6, 2008 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-20300288
16.
Bloom's syndrome in a 12-year-old Iranian girl.
Indian J Hum Genet
; 14(3): 103-5, 2008 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-20300305
17.
Serum level of anti-mullerian hormone in early follicular phase as a predictor of ovarian reserve and pregnancy outcome in assisted reproductive technology cycles.
Arch Iran Med
; 11(4): 371-6, 2008 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-18588367
18.
Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.
Biomed Res Int
; 2018: 3103986, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29568747
19.
Pattern of menarche age (normal, early and late) and its relationship with some demographic characteristics in girls and their parents.
Int J Adolesc Med Health
; 30(3)2016 Aug 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-27564696
20.
Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families.
Orphanet J Rare Dis
; 9: 108, 2014 Jul 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-25231166