Possible narrowed assignment of the loci of monosomy 21-associated microcephaly and intrauterine growth retardation to a 1.2-Mb segment at 21q22.2.
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Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literatureDyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in miceDistinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A.Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportGene dosage-dependent association of DYRK1A with the cytoskeleton in the brain and lymphocytes of down syndrome patients.Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.One-carbon cycle alterations induced by Dyrk1a dosage.Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.
P2860
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P2860
Possible narrowed assignment of the loci of monosomy 21-associated microcephaly and intrauterine growth retardation to a 1.2-Mb segment at 21q22.2.
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1997 nî lūn-bûn
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Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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P2093
P2860
P1476
Possible narrowed assignment o ...... o a 1.2-Mb segment at 21q22.2.
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P2093
P2860
P304
P407
P577
1997-04-01T00:00:00Z