X-chromosome linked inheritance of decreased thyroxine-binding globulin

Ten-year outcomes after primary vertical sleeve gastrectomy for morbid obesity: a monocentric cohort study.

Surgical endoscopy·2020

Risk factors of perioperative morbimortality after laparoscopic sleeve gastrectomy: a club coelio multicenter study.

Acta chirurgica Belgica·2017

Assessment of predictive factors for recurrence in laparoscopic ventral hernia repair using a bridging technique.

Surgical endoscopy·2017

Incisional hernia after single-incision laparoscopic cholecystectomy: incidence and predictive factors.

Surgical endoscopy·2016

Fibrosis of the thyroid gland caused by an IgG4-related sclerosing disease: three years of follow-up.

Acta clinica Belgica·2014

Comparison between single incision and conventional laparoscopic cholecystectomy for uncomplicated cholelithiasis.

Acta chirurgica Belgica·2014

Impacts of vaping on children and young people: a systematic review.

Archives of disease in childhood·2026

Informed, autonomous and safe: a qualitative study describing the views of English adolescents on consent to participate in medical research.

Archives of disease in childhood·2026

National variations within the timings of transport to paediatric intensive care from 2018 to 2022: a cohort study.

Archives of disease in childhood·2026

Using directed acyclic graphs in observational research: a practical guide for paediatric researchers.

Archives of disease in childhood·2026

Timing and incidence of health conditions recorded during childhood in White British and Pakistani British children: evidence from the Born in Bradford cohort.

Archives of disease in childhood·2026

Trends in neonatal mortality and morbidity at a tertiary centre over four decades: a cohort study.

Archives of disease in childhood·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Related Experiment Videos

X-chromosome linked inheritance of decreased thyroxine-binding globulin

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Ten-year outcomes after primary vertical sleeve gastrectomy for morbid obesity: a monocentric cohort study.

Risk factors of perioperative morbimortality after laparoscopic sleeve gastrectomy: a club coelio multicenter study.

Assessment of predictive factors for recurrence in laparoscopic ventral hernia repair using a bridging technique.

Incisional hernia after single-incision laparoscopic cholecystectomy: incidence and predictive factors.

Fibrosis of the thyroid gland caused by an IgG4-related sclerosing disease: three years of follow-up.

Comparison between single incision and conventional laparoscopic cholecystectomy for uncomplicated cholelithiasis.

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Timing and incidence of health conditions recorded during childhood in White British and Pakistani British children: evidence from the Born in Bradford cohort.

Trends in neonatal mortality and morbidity at a tertiary centre over four decades: a cohort study.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

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X-chromosome linked inheritance of decreased thyroxine-binding globulin

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