The phenotype of Floating–Harbor syndrome in 10 patients

The phenotype of Floating–Harbor syndrome in 10 patients

Source :

• American Journal of Medical Genetics Part A [ 1552-4825 ] ; 2010-04.

Descripteurs français

• Pascal (Inist)
  • Homme, Malade, Phénotype, Retard langage, Retard staturopondéral.
• Wicri :
  • topic : Homme, Petite enfance, Génétique.

English descriptors

• KwdEn :
  • Abnormality, Adult height, Adult heights, Adult life, American journal, Array analysis, Australia department, Behavioral phenotype, Behavioral problems, Biomedical research centre, Birth weight, Body habitus, Case report, Celiac disease, Centile, Centile birth length, Cerebral aneurysm, Clavicular pseudarthrosis, Clinical features, Conductive hearing loss, Consonant imprecision, Current height, Dental problems, Different ages, Dysmorphic features, Dysmorphism, Dysplastic hips, Dyspraxia, Early childhood, Early intervention, Early puberty, Educational reports, Facial, Facial appearance, Facial features, Feingold, Floatingharbor syndrome, Fryns, Genet, Genet part, Genetic health services victoria, Genetics, Growth hormone, Growth hormone treatment, Growth retardation, Growth velocity, Hand abnormalities, Hand dysmorphism, Health problems, High frequency, Human, Impairment, Intellectual disability, Intellectual education, Intellectual function, Lacombe, Language disorder, Language retardation, Mainstream, Mainstream school, Medical genetics part, Microarray analysis, Months patient, Motor speech production, Online issue, Original patients, Other reports, Oxford partnership, Patient, Patient cohort, Patient group, Peippo, Pharyngeal wall, Phenotype, Precocious puberty, Previous case reports, Previous reports, Puberty, Royal hospital, Same patient, Serial bone, Several patients, Severe disorder, Short palpebral, Short stature, Skeletal abnormalities, Speech delay, Syndrome, Syndrome diagnosis, Typical body habitus, Verbal dyspraxia, Wide mouth, Years patient.
• Teeft :
  • Abnormality, Adult height, Adult heights, Adult life, American journal, Array analysis, Australia department, Behavioral phenotype, Behavioral problems, Biomedical research centre, Birth weight, Body habitus, Case report, Celiac disease, Centile, Centile birth length, Cerebral aneurysm, Clavicular pseudarthrosis, Clinical features, Conductive hearing loss, Consonant imprecision, Current height, Dental problems, Different ages, Dysmorphic features, Dysmorphism, Dysplastic hips, Dyspraxia, Early childhood, Early intervention, Early puberty, Educational reports, Facial, Facial appearance, Facial features, Feingold, Floatingharbor syndrome, Fryns, Genet, Genet part, Genetic health services victoria, Genetics, Growth hormone, Growth hormone treatment, Growth velocity, Hand abnormalities, Hand dysmorphism, Health problems, High frequency, Impairment, Intellectual disability, Intellectual education, Intellectual function, Lacombe, Language disorder, Mainstream, Mainstream school, Medical genetics part, Microarray analysis, Months patient, Motor speech production, Online issue, Original patients, Other reports, Oxford partnership, Patient cohort, Patient group, Peippo, Pharyngeal wall, Phenotype, Precocious puberty, Previous case reports, Previous reports, Puberty, Royal hospital, Same patient, Serial bone, Several patients, Severe disorder, Short palpebral, Short stature, Skeletal abnormalities, Speech delay, Syndrome, Syndrome diagnosis, Typical body habitus, Verbal dyspraxia, Wide mouth, Years patient.

Abstract

• https://api.istex.fr/document/0F6B0004F6751FD400BDABFB9A448EAE41F0C8B8/fulltext/pdf

Affiliations:

• Australie, France, Royaume-Uni
• Angleterre, Aquitaine, Nouvelle-Aquitaine, Oxfordshire, Victoria (État)
• Bordeaux, Melbourne, Oxford
• Université d'Oxford, Université de Bordeaux, Université de Melbourne

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