https://www.jci.org/articles/view/166275/pdf
JCI - Loss of Mtm1 causes cholestatic liver disease in a model of X-linked myotubular myopathy
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https://teletype.in/@kumarlakshayman/oTu_KeQig
Report: The Impact of COVID-19 on Global X-linked Hypophosphatemia Market, Projected Fact.MR —...
Apr 22, 2020 - X-Linked hypophosphatemia (XLH) refers to an inherited disorder characterized by low phosphate concentration in the blood. The therapy...
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https://www.ern-eye.eu/ern-eye-webinar-x-linked-retinoschisis/
ERN-EYE Webinar - X-linked retinoschisis - ERN-EYE
ERN-EYE Webinar - X-linked retinoschisis Date and time Friday 30 October, 2.00 pm CET. Programme Clinical Characteristics, Dr Joni Turunen, HUS Helsinki...
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https://eyecarecenteroc.com/en/conditions/x-linked-juvenile-retinoschisis/irvine
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X-Linked Juvenile Retinoschisis treatment in Irvine, CA. Early diagnosis improves outcomes. Regular comprehensive eye examinations. Call (949) 323-3600.
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https://www.longdom.org/open-access/xlinked-agammaglobulinemia--is-it-really-rare-2572-0775-1000130.pdf
X-linked Agammaglobulinemia - Is it Really Rare?
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https://www.ace-hta.gov.sg/healthcare-professionals/ace-technology-guidance/drug-guidance/burosumab-for-treating-x-linked-hypophosphataemia/
Burosumab for treating X-linked hypophosphataemia | Agency for Care Effectiveness
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https://yonsei.elsevierpure.com/en/publications/genotypephenotype-correlations-in-83-korean-x-linked-retinoschisi/fingerprints/
Genotype–Phenotype Correlations in 83 Korean X-linked Retinoschisis Patients: Impact of...
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https://www.pearson.com/channels/biology/asset/62436534/x-linked-recessive-disorder-hemophilia-inheritance
X-Linked Recessive Disorder: Hemophilia Inheritance | Study Prep in Pearson+
X-Linked Recessive Disorder: Hemophilia Inheritance
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https://kidsfirstdrc.org/publication/x-linked-genetic-associations-in-sporadic-thoracic-aortic-dissection/
X-linked genetic associations in sporadic thoracic aortic dissection - Kids First
Apr 23, 2026 - The male predominance in sporadic thoracic aortic aneurysm and dissection (TAD) suggests that the X chromosome contributes to TAD, but this has not been...
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https://cris.haifa.ac.il/en/publications/aro81-a-polymorphic-x-linked-bovine-microsatellite/
ARO81: A polymorphic X-linked bovine microsatellite - University of Haifa
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https://www.danonfoundation.org/resource/primary-lamp-2-deficiency-causes-x-linked-vacuolar-cardiomyopathy-and-myopathy-danon-disease/
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease) -...
Oct 18, 2025 - Primary LAMP2 deficiency causes cardiomyopathy and myopathy (Danon Disease).
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https://rememberthegirls.org/uniting-women-with-x-linked-disorders-to-prompt-change/
Uniting women with X-linked disorders to prompt change - Remember The Girls
May 15, 2025 - An article written by G Shellye Horowitz featuring Taylor Kane, the founder of Remember The Girls, and her inspiration for the organization.
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https://www.atasehirgenetik.com.tr/genetik-test/6336fa9107fdc
Özel Ataşehir Genetik - Hypospadias 1, X-linked Testi
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https://www.letstalkacademy.com/x-linked-agammaglobulinemia-btk-gene-mutation/
X-linked Agammaglobulinemia: Role of BTK Gene Mutation
Apr 15, 2025 - Learn about X-linked agammaglobulinemia, an immunodeficiency caused by a mutation in the BTK gene. Discover the importance of this mutation and its impact on...
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https://ekjo.org/journal/view.php?viewtype=pubreader&number=466
A Novel Mutation in the XLRS1 Gene in a Korean Family with X-linked Retinoschisis
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https://avehjournal.org/index.php/aveh/article/view/522/1092
X-linked juvenile retinoschisis in a black South African: A case report | Rafferty | African Vision...
The African Vision and Eye Health journal publishes original peer-reviewed papers of scientific and clinical research in optometry, ophthalmology, vision...
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https://www.ispor.org/heor-resources/presentations-database/presentation-cti/ispor-europe-2025/poster-session-2-2/cost-utility-analysis-of-including-x-linked-adrenoleukodystrophy-in-the-spanish-newborn-screening-program
ISPOR - Cost-Utility Analysis of Including X-linked Adrenoleukodystrophy in the Spanish Newborn...
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https://hemoncim.com/jour/article/view/144/144/en_US
X-Linked lymphoproliferative syndrome types 1 and 2 (Review of literature and clinical case...
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https://iscrm.uw.edu/recent_research/g-p-41-canine-x-linked-myotubular-myopathy-a-dose-finding-study-of-systemic-aav8-mtm1-effects-on-muscle-strength-gait-respiration-neuromuscular-function-and-survival/
G.P.41: Canine X-linked myotubular myopathy: A dose-finding study of systemic AAV8-MTM1 effects on...
Jul 2, 2018 - Neuromuscular Disorders, October 2014
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https://avesis.sdu.edu.tr/yayin/c5a24cfe-8a12-46b2-90b1-c93ca69fb300/x-linked-spinal-and-bulbar-muscular-atrophy-without-proximal-atrophy
X-linked spinal and bulbar muscular atrophy without proximal atrophy | AVESİS
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https://pure.psu.edu/en/publications/x-linked-inhibitor-of-apoptosis-protein-inhibits-apoptosis-in-inf/
X-linked inhibitor of apoptosis protein inhibits apoptosis in inflammatory breast cancer cells with...
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https://www.cgtlive.com/view/biogen-biib112-gene-therapy-falls-short-in-x-linked-retinitis-pigmentosa
Biogen's BIIB112 Gene Therapy Falls Short in X-Linked Retinitis Pigmentosa | CGTlive®
Oct 8, 2026 - Although the XIRIUS study did not meet its primary end point, positive trends were observed across several clinically relevant prespecified secondary end...
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https://pure.johnshopkins.edu/en/publications/x-linked-adrenoleukodystrophy-pathology-pathophysiology-diagnosti/
X-linked adrenoleukodystrophy: Pathology, pathophysiology, diagnostic testing, newborn screening...
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https://academicworks.cuny.edu/hc_pubs/425/
"Can colour vision re-evolve? Variation in the X-linked opsin locus of " by N. I. Mundy, N. C....
Background: Do evolutionary specializations lead to evolutionary constraint? This appears plausible, particularly when specialization leads to loss of complex...
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https://checkorphan.org/disease/thrombocytopenia-x-linked/
Thrombocytopenia X-linked – CheckOrphan
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https://newbornscreening.hrsa.gov/conditions/x-linked-adrenoleukodystrophy
X-Linked Adrenoleukodystrophy | Newborn Screening
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https://teachrare.org/raising-awareness-female-carriers-of-x-linked-rare-diseases/
Raising Awareness of Female Carriers of X-Linked Rare Diseases - Teach RARE
Jan 19, 2025 - Non-profit aims to raise awareness and support for female carriers of X-linked rare diseases, focused support for women with a rare disease.
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https://avesis.uludag.edu.tr/yayin/736ec7ce-fc05-4aa9-bd73-1bf489c1947e/expansion-of-myeloid-derived-suppressor-cells-in-patients-with-x-linked-agammaglobulinemia
EXPANSION OF MYELOID-DERIVED SUPPRESSOR CELLS IN PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA | AVESİS
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https://dnalabsindia.com/test/ophn1-gene-mental-retardation-x-linked-with-cerebellar-hypoplasia-and-distinctive-facial-appearance-ngs-genetic-dna-test
OPHN1 Gene Mental retardation, X-linked, with… | ISO 9001:2015 | DNA Labs India
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https://www.pombase.org/term/MONDO:0010355
PomBase - Disease association ontology term - MONDO:0010355 - syndromic X-linked intellectual...
PomBase - Disease association ontology term - MONDO:0010355 - syndromic X-linked intellectual disability Claes-Jensen type - The Schizosaccharomyces pombe...
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https://scholars.uthscsa.edu/en/publications/spastic-paraplegia-with-iron-deposits-in-the-basal-ganglia-a-new-/
Spastic paraplegia with iron deposits in the basal ganglia: A new X-linked mental retardation...
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https://openophthalmologyjournal.com/VOLUME/15/PAGE/201/ABSTRACT/
X-linked Retinoschisis Associated with Retinitis Punctata Albescens Caused by a Mutation in the RS1...
X-linked Retinoschisis Associated with Retinitis Punctata Albescens Caused by a Mutation in the RS1 Gene: A Family Study
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https://3d-hub-organoids.com/dynamic-allele-usage-of-x-linked-genes-ameliorates-neurodevelopmental-disease-phenotypes-in-brain-organoids/
Dynamic allele usage of X-linked genes ameliorates neurodevelopmental disease phenotypes in brain...
Jan 15, 2026 - Nat Commun. 2026 Jan 14. doi: 10.1038/s41467-026-68428-x. Online ahead of print. ABSTRACT While random X-chromosome inactivation in female cells of placental...
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https://www.patlynk.com/fr/trial/NCT00004827
Study of Docosahexaenoic Acid (DHA) Supplementation in Patients With X-Linked Retinitis Pigmentosa...
PROTOCOL OUTLINE: This is a randomized, parallel, double blind study. Patients receive 2 gel capsules per day of either docosahexaenoic acid (DHA) enriched oil
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https://explority.ai/diseases/3063
X-linked intellectual disability, Snyder type: Research & Drug Discovery Data
X-linked intellectual disability, Snyder type: population, burden, unmet need, standard of care gaps, market, latest research, and drug candidates in...
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https://genprice.com/protein-antibody-binding/recombinant-human-rna-binding-motif-protein-x-linked-like-1-c-his-4035781430687
Recombinant Human RNA binding motif protein, X-linked-like-1 (C-His) | Genprice
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https://www.artikata.com/arti-205527-x-linked+scid.html
Definisi: x-linked scid, Arti Kata: x-linked scid
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https://metabolicsupport.org/condition/x-linked-hypophosphataemia/
X-linked Hypophosphataemia - Metabolic Support
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https://experts.umn.edu/en/publications/diffusion-tensor-brain-mr-imaging-in-x-linked-cerebral-adrenoleuk/fingerprints/?sortBy=alphabetically
Diffusion tensor brain MR imaging in X-linked cerebral adrenoleukodystrophy - Fingerprint -...
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https://araceagainstblindness.org/education/blog/research-42795865-micropulse-laser-in-x-linked-retinoschisis-early-findings-from-two-brothers
Micropulse Laser in X-Linked Retinoschisis: Early Findings from Two Brothers | A Race Against...
A two-patient study explored subthreshold micropulse laser in brothers with molecularly confirmed X-linked retinoschisis. The treatment was feasible and sh
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https://scientificorigin.com/tag/x-linked-agammaglobulinemia
X-linked Agammaglobulinemia Archives | ScientificOrigin
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https://publikationen.uni-tuebingen.de/xmlui/handle/10900/118972
X-Linked Retinitis Pigmentosa Caused by Non-Canonical Splice Site Variants in RPGR
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https://www.cgtlive.com/view/x-linked-retinitis-pigmentosa-trial-exceeds-enrollment
X-Linked Retinitis Pigmentosa Trial Exceeds Enrollment | CGTlive®
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https://profiles.foxchase.org/en/publications/the-x-linked-mental-retardation-gene-smcxjarid1c-defines-a-family/
The X-Linked Mental Retardation Gene SMCX/JARID1C Defines a Family of Histone H3 Lysine 4...
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https://iris.uniupo.it/handle/11579/193744
G-quadruplexes in an SVA retrotransposon cause aberrant TAF1 gene expression in X-linked dystonia...
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https://www.bx.psu.edu/makova_lab/publication/2011-06-biol_direct/
A computational approach to candidate gene prioritization for X-linked mental retardation using...
Jun 1, 2011 - Several computational candidate gene selection and prioritization methods have recently been developed. These in silico selection and prioritization techniques...
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https://pure.fujita-hu.ac.jp/ja/publications/a-novel-col4a5-splicing-variant-causing-x-linked-alport-syndrome-/
A novel COL4A5 splicing variant causing X-linked Alport syndrome: A case report - 藤田医科大学
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https://volv.global/diseases/x-linked-hypophosphataemia/
X-Linked Hypophosphataemia (XLH): Symptoms & Diagnosis
X-Linked Hypophosphataemia (XLH): a hereditary phosphate-wasting disorder causing rickets and osteomalacia. Symptoms, prevalence and why adults go undiagnosed.
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https://erorin.net/tag/x-linked-diseases
X-linked diseases - erorin.net
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https://perfilesycapacidades.javeriana.edu.co/es/publications/linkage-mapping-of-a-large-colombian-family-segregating-for-x-lin/
Linkage mapping of a large Colombian family segregating for X linked retinoschisis: Refinement of...
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https://iris.univr.it/handle/11562/4016
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene
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https://avesis.istanbul.edu.tr/yayin/e411c903-1db0-419e-8766-54fa9d017a77/mutation-update-for-kabuki-syndrome-genes-kmt2d-and-kdm6a-and-further-delineation-of-x-linked-kabuki-syndrome-subtype-2
Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked...
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https://www.hslpathology.com/services/hsl-genetics/tests/nystagmus-x-linked-infantile-frmd7-gene-sequencing/
Nystagmus, X-linked Infantile – FRMD7 gene sequencing | Health Services Laboratories
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