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Arthritis Research & Therapy|April 19, 2022
Lupus nephritis correlates with B cell interferon-β, anti-Smith, and anti-DNA: a retrospective studyFatima Alduraibi, Huma Fatima, Jennie A Hamilton, et al.
Pakistan Journal of Medical Sciences|June 21, 2014
Study of non-syndromic thumb aplasia in six independent casesHafiza Fizzah Riaz, Karmoon Lal, Bashir Ahmad, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|June 10, 2026
Hydrocele of the canal of nuck: a case series and literature reviewChristopher Co, Sujith Wijerathne, Leonil Dacaynos, et al.
European Journal of Human Genetics : EJHG|March 28, 2018
Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertilityYeşerin Yıldırım, Toufik Ouriachi, Ute Woehlbier, et al.
European Journal of Medical Genetics|March 1, 2021
CRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomaliesMine Koprulu, Rana Muhammad Kamran Shabbir, Qamar Zaman, et al.
The Yale Journal of Biology and Medicine|October 2, 2023
A Recurrent Mutation in Growth Hormone Receptor (GHR) Gene Underlying Laron-type Dwarfism in a Pakistani FamilyRana Muhammad Kamran Shabbir, Gökhan Nalbant, Qamar Zaman, et al.
Pakistan Journal of Medical Sciences|May 17, 2016
Phenotypic manifestation of congenital transverse amputation of autopod in Pakistani subjectsHafiza Fizzah Riaz, Karmoon Lal, Saif Ullah, et al.
Pakistan Journal of Medical Sciences|November 18, 2024
Burden of congenital and hereditary anomalies and their epidemiological attributes in the pediatric and adult population of Peshawar valley, PakistanSyeda Farwa Naqvi, Umi Ameena, Waheed Uddin Qazi, et al.
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