Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes

Q1

EUROPEAN JOURNAL OF HUMAN GENETICS (ISSN: 10184813) , vol. 30 , pp. 219-228

Differences in thrombin and plasmin generation potential between East African and Western European adults: The role of genetic and non-genetic factors

Q1

JOURNAL OF THROMBOSIS AND HAEMOSTASIS (ISSN: 15387933) , vol. 20 , pp. 1089-1105

Clinical lesson learned from genetic analysis in patients prior to surgical repair of hypospadias

Q1

ASIAN JOURNAL OF UROLOGY (ISSN: 22143882) , vol. 9 , pp. 186-189

Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries

Q2

CLINICAL ENDOCRINOLOGY (ISSN: 03000664)

Osteogenic transdifferentiation of primary human fibroblasts to osteoblast-like cells with human platelet lysate

Q1

SCIENTIFIC REPORTS , vol. 12

Genetic Analysis Reveals Complete Androgen Insensitivity Syndrome in Female Children Surgically Treated for Inguinal Hernia

Q2

JOURNAL OF INVESTIGATIVE SURGERY (ISSN: 08941939) , vol. 34 , pp. 227-233

Analysis of the androgen receptor (AR) gene in a cohort of Indonesian undermasculinized 46, XY DSD patients

Q4

EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS (ISSN: 11108630) , vol. 22

Surveillance and prevalence of fragile X syndrome in Indonesia

Q2

INTRACTABLE AND RARE DISEASES RESEARCH (ISSN: 21863644) , vol. 10 , pp. 11-16

Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individuals

Q2

SINGAPORE MEDICAL JOURNAL (ISSN: 00375675) , vol. 62 , pp. 143-148

Clinical manifestation and genetic analysis of familial rare disease genodermatosis xeroderma pigmentosum

Q2

INTRACTABLE AND RARE DISEASES RESEARCH (ISSN: 21863644) , vol. 10 , pp. 114-121