Genotype-Phenotype Correlates in Fragile X Syndrome

Journal of Child and Adolescent Behaviour ◽

10.4172/2375-4494.1000368 ◽

2018 ◽

Vol 06 (01) ◽

Author(s):

Eman Ahmed Zaky

Keyword(s):

Fragile X Syndrome ◽

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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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