Works matching IS 03406717 AND DT 2006 AND VI 118 AND IP 5
Results: 13
A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.
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- Human Genetics, 2006, v. 118, n. 5, p. 640, doi. 10.1007/s00439-005-0081-1
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- Article
Population stratification confounds genetic association studies among Latinos.
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- Human Genetics, 2006, v. 118, n. 5, p. 652, doi. 10.1007/s00439-005-0071-3
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- Article
Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a ∼0.5-Mb submicroscopic deletion in a patient with mild mental retardation.
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- 2006
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- Correction Notice
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3.
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- Human Genetics, 2006, v. 118, n. 5, p. 665, doi. 10.1007/s00439-005-0086-9
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- Article
Admixture-matched case-control study: a practical approach for genetic association studies in admixed populations.
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- Human Genetics, 2006, v. 118, n. 5, p. 626, doi. 10.1007/s00439-005-0080-2
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- Article
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.
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- Human Genetics, 2006, v. 118, n. 5, p. 618, doi. 10.1007/s00439-005-0077-x
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- Article
Ring chromosome 15: characterization by array CGH.
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- Human Genetics, 2006, v. 118, n. 5, p. 611, doi. 10.1007/s00439-005-0030-z
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- Article
A novel autosomal recessive non-syndromic hearing impairment locus ( DFNB47) maps to chromosome 2p25.1-p24.3.
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- Human Genetics, 2006, v. 118, n. 5, p. 605, doi. 10.1007/s00439-005-0079-8
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- Article
Contrasting patterns of Y-chromosome variation in South Siberian populations from Baikal and Altai-Sayan regions.
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- Human Genetics, 2006, v. 118, n. 5, p. 591, doi. 10.1007/s00439-005-0076-y
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- Article
Variation in genes involved in the RANKL/RANK/OPG bone remodeling pathway are associated with bone mineral density at different skeletal sites in men.
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- Human Genetics, 2006, v. 118, n. 5, p. 568, doi. 10.1007/s00439-005-0062-4
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- Article
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.
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- Human Genetics, 2006, v. 118, n. 5, p. 578, doi. 10.1007/s00439-005-0072-2
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- Article
Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy.
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- Human Genetics, 2006, v. 118, n. 5, p. 559, doi. 10.1007/s00439-005-0084-y
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- Article
The neurobeachin gene spans the common fragile site FRA13A.
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- Human Genetics, 2006, v. 118, n. 5, p. 551, doi. 10.1007/s00439-005-0083-z
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- Article