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1 Ergebnisse
1
Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in frag..:
Tassanakijpanich, Nattaporn
;
McKenzie, Forrest J
;
McLennan, Yingratana A
...
qt67c0975f. , 2022
Link:
https://escholarship.org/uc/item/67c0975f
RT Journal T1
Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt67c0975f&Exemplar=1&LAN=DE A1 Tassanakijpanich, Nattaporn A1 McKenzie, Forrest J A1 McLennan, Yingratana A A1 Makhoul, Elisabeth A1 Tassone, Flora A1 Jasoliya, Mittal J A1 Romney, Christopher A1 Petrasic, Ignacio Cortina A1 Napalinga, Kaye A1 Buchanan, Caroline B A1 Hagerman, Paul A1 Hagerman, Randi A1 Casanova, Emily L PB eScholarship, University of California YR 2022 K1 Intellectual and Developmental Disabilities (IDD) K1 Pediatric K1 Genetics K1 Brain Disorders K1 Fragile X Syndrome K1 Rare Diseases K1 Child K1 Preschool K1 Ehlers-Danlos Syndrome K1 Female K1 Fragile X Mental Retardation Protein K1 Heterozygote K1 Humans K1 Male K1 Phenotype K1 Trinucleotide Repeat Expansion K1 genetic predisposition to disease K1 medical K1 human genetics K1 gene expression K1 Biological Sciences K1 Medical and Health Sciences K1 Genetics & Heredity JF qt67c0975f LK http://dx.doi.org/https://escholarship.org/uc/item/67c0975f DO https://escholarship.org/uc/item/67c0975f SF ELIB - SuUB Bremen
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