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A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family
by
Moghadasi, Setareh
,
van Haeringen, Arie
,
Langendonck, Lieke
,
Gijsbers, Antoinet C. J.
,
Ruivenkamp, Claudia A. L.
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics. Part A
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Subjects
3P26 Deletion Syndrome
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Adult
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Aged, 80 And Over
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Chromosome Deletion
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Chromosomes, Human, Pair 3
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Female
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Genetic Counseling
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Genetics & Heredity
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Genome-Wide Association Study
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Humans
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In Situ Hybridization, Fluorescence
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Infant
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Intellectual Disability - Diagnosis
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Intellectual Disability - Genetics
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Life Sciences & Biomedicine
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Male
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Middle Aged
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Pedigree
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Phenotype
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Polymorphism, Single Nucleotide
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