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Jacobsen syndrome: MedlinePlus Genetics
- https://medlineplus.gov/genetics/condition/jacobsen-syndrome/
- Jacobsen syndrome is a condition caused by a loss of genetic material from chromosome 11. Because this deletion occurs at the end (terminus) of the long (q) arm of …
Jacobsen syndrome - National Organization for Rare …
- https://rarediseases.org/gard-rare-disease/jacobsen-syndrome/
- Overview. Jacobsen syndrome is a condition characterized by the deletion of several genes on chromosome 11. Signs and symptoms vary among affected people but often …
Jacobsen syndrome - Living with the Disease - Genetic …
- https://rarediseases.info.nih.gov/diseases/307/jacobsen-syndrome/living/
- National Organization of Rare Disorders (NORD): Jacobsen syndrome Provides information about rare diseases for patients and families through consultation with …
Jacobsen Syndrome ( JBS ) - MalaCards
- https://www.malacards.org/card/jacobsen_syndrome
- OMIM®: 57 Jacobsen syndrome (JBS) is a contiguous gene deletion syndrome with major clinical features of growth retardation, psychomotor retardation, trigonocephaly, …
Jacobsen syndrome - About the Disease - Genetic and …
- https://rarediseases.info.nih.gov/diseases/307/jacobsen-syndrome/
- Jacobsen syndrome is a condition characterized by the deletion of several genes on chromosome 11. Signs and symptoms vary among affected people but often include …
Jacobsen Syndrome - Physiopedia
- https://www.physio-pedia.com/Jacobsen_Syndrome
- Jacobsen syndrome is a chromosomal disorder in which children with JS will have a global developmental delays, presented by delayed motor and speech milestones. …
Jacobsen syndrome | Contact
- https://contact.org.uk/conditions/jacobsen-syndrome/
- In Jacobsen syndrome, a small piece of the 11th chromosome is deleted (or missing) and this causes a range of clinical features in individuals with this condition. The …
Jacobsen Syndrome Medical Assistance | Day of Difference
- https://dayofdifference.org.au/j-medical/jacobsen-syndrome-medical-assistance.html
- Jacobsen syndrome is a rare chromosomal disorder resulting from deletion of genes from chromosome 11 that includes band 11q24.1. It is a congenital disorder. Since the deletion …
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