"Autosomal dominant disorder" trang 1 - tải miễn phí từ tailieunhanh
Familial achalasia with an autosomal dominant pattern of inherence: Report of a Vietnamese family

Familial achalasia with an autosomal dominant pattern of inherence: Report of a Vietnamese family
4    56    1
Nonselective cyclooxygenase inhibition retards cyst progression in a murine model of autosomal dominant polycystic kidney disease

Nonselective cyclooxygenase inhibition retards cyst progression in a murine model of autosomal dominant polycystic kidney disease
9    68    0
UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: A pediatric case report and literature review

UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: A pediatric case report and literature review
5    106    0
Identification of a mutation in a Vietnamese family with autosomal dominant polycystic kidney disease using whole exome sequencing

Identification of a mutation in a Vietnamese family with autosomal dominant polycystic kidney disease using whole exome sequencing
7    4    1
Autosomal dominant polycystic kidney disease with ectopic unilateral multicystic kidney: A case report

Autosomal dominant polycystic kidney disease with ectopic unilateral multicystic kidney: A case report
4    6    1
Ebook USMLE road map - Genetics: Part 1

Ebook USMLE road map - Genetics: Part 1
80    124    1
Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors

Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors
12    56    1
Báo cáo y học:

Báo cáo y học: " Autosomal dominant polycystic kidney disease with diffuse proliferative glomerulonephritis - an unusual association: a case report and review of the literature"
5    78    0
Constitutional delay of puberty: Presentation and inheritance pattern in 48 familial cases

Constitutional delay of puberty: Presentation and inheritance pattern in 48 familial cases
8    92    0
HDR syndrome in a Japanese girl with biliary atresia: A case report

HDR syndrome in a Japanese girl with biliary atresia: A case report
4    99    0
Case report of ascending colon cancer and multiple jejunal GISTs in a patient with neurofibromatosis type 1 (NF1)

Case report of ascending colon cancer and multiple jejunal GISTs in a patient with neurofibromatosis type 1 (NF1)
6    60    0
Laryngo-tracheal stenosis in a woman with ablepharon macrostomia syndrome

Laryngo-tracheal stenosis in a woman with ablepharon macrostomia syndrome
4    50    1
Birt–Hogg–Dubé syndrome: A literature review and case study of a Chinese woman presenting a novel FLCN mutation

Birt–Hogg–Dubé syndrome: A literature review and case study of a Chinese woman presenting a novel FLCN mutation
6    18    1
The negative charge of the 343 site is essential for maintaining physiological functions of CXCR4

The negative charge of the 343 site is essential for maintaining physiological functions of CXCR4
10    19    1
Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation

Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation
11    10    1
Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases

Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases
7    12    1
Waardenburg syndrome type 4 coexisting with open-angle glaucoma: A case report

Waardenburg syndrome type 4 coexisting with open-angle glaucoma: A case report
11    1    1
Ebook Endocrine FGFs and Klothos

Ebook Endocrine FGFs and Klothos
250    1    1
Ebook Endocrine FGFs and Klothos

Ebook Endocrine FGFs and Klothos
250    1    1
Autosomal dominant transmission of transient neonatal lactic acidosis: A case report

Autosomal dominant transmission of transient neonatal lactic acidosis: A case report
4    86    0