Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems

JAMA Network Open ◽

10.1001/jamanetworkopen.2021.41516 ◽

2021 ◽

Vol 4 (12) ◽

pp. e2141516

Author(s):

Arezoo Movaghar ◽

David Page ◽

Murray Brilliant ◽

Marsha Mailick

Keyword(s):

Fragile X Syndrome ◽

Health Systems ◽

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Monozygotic boys with fragile X syndrome, DMCN 42: 768–74

Developmental Medicine & Child Neurology ◽

10.1017/s0012162201250269 ◽

2001 ◽

Vol 43 (02) ◽

pp. 142

Keyword(s):

Fragile X Syndrome ◽

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Fragile X syndrome, mental retardation and macroorchidism

Clinical Genetics ◽

10.1034/j.1399-0004.1998.5440420.x ◽

1998 ◽

Vol 54 (4) ◽

pp. 366-367

Keyword(s):

Mental Retardation ◽

Fragile X Syndrome ◽

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Living with Fragile X Syndrome

10.33015/dominican.edu/2017.ot.05 ◽

2017 ◽

Author(s):

◽

Rebecca Schira ◽

Samantha Alexander ◽

Noelani Brisbane ◽

Kaitlyn Williams

Keyword(s):

Fragile X Syndrome ◽

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Effects of Sertraline Treatment for Young Children with Fragile X Syndrome: Family Perspectives via Case Studies

10.33015/dominican.edu/2019.ot.01 ◽

2019 ◽

Author(s):

◽

Tracy Ye ◽

Decerie Mendoza ◽

Elena Javier ◽

Martina Dualan

Keyword(s):

Young Children ◽

Case Studies ◽

Fragile X Syndrome ◽

Fragile X ◽

Family Perspectives

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Fragile X Syndrome and Family Occupations

10.33015/dominican.edu/2019.ot.rp.02 ◽

2019 ◽

Author(s):

Decerie Mendoza ◽

Tracy Ye ◽

Martina Dualan ◽

Elena Javier

Keyword(s):

Fragile X Syndrome ◽

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Successful Polar Body-based Preimplantation genetic diagnosis for Fragile-X syndrome and Gaucher Disease

10.26226/morressier.5912d9ebd462b802923864ac ◽

2017 ◽

Author(s):

Marina Bellavia

Keyword(s):

Fragile X Syndrome ◽

Preimplantation Genetic Diagnosis ◽

Gaucher Disease ◽

Fragile X ◽

Genetic Diagnosis

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Introducing direct CGG repeat analysis in preimplantation genetic diagnosis (PGD) for fragile X syndrome: an overview of clinical outcomes for 116 patients

10.26226/morressier.5af300b2738ab10027aa98fe ◽

2018 ◽

Author(s):

Rachael Cabey

Keyword(s):

Fragile X Syndrome ◽

Clinical Outcomes ◽

Preimplantation Genetic Diagnosis ◽

Fragile X ◽

Genetic Diagnosis ◽

Repeat Analysis

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Orphan designation: N-[(1R)-1-phenylethyl]-6-{1H-pyrazolo[3,4-d]pyrimidin-4-yl}quinazolin-2-amine, Treatment of fragile X syndrome

Case Medical Research ◽

10.31525/cmr-fa7181 ◽

2019 ◽

Author(s):

Keyword(s):

Fragile X Syndrome ◽

Fragile X ◽

Orphan Designation

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Orphan designation: Tideglusib, Treatment of fragile X syndrome

Case Medical Research ◽

10.31525/cmr-bd6493 ◽

2019 ◽

Author(s):

Keyword(s):

Fragile X Syndrome ◽

Fragile X ◽

Orphan Designation

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A Trial of Metformin in Individuals With Fragile X Syndrome (Met)

Case Medical Research ◽

10.31525/ct1-nct03862950 ◽

2019 ◽

Author(s):

Keyword(s):

Fragile X Syndrome ◽

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