Works matching IS 14345161 AND DT 2001 AND VI 46 AND IP 3
Results: 13
Fetal cells in transcervical samples at an early stage of gestation.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 99, doi. 10.1007/s100380170095
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Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 105, doi. 10.1007/s100380170096
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Screening for deletions in interval D16-22 of the Y chromosome in azoospermic and oligozoospermic Japanese men.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 110, doi. 10.1007/s100380170097
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Mitochondrial DNA polymorphisms in Thailand.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 115, doi. 10.1007/s100380170098
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X chromosome inactivation patterns in 45,X/46,XX mosaics.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 126, doi. 10.1007/s100380170099
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Human calcitonin receptor-like receptor for adrenomedullin: genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 132, doi. 10.1007/s100380170100
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Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 137, doi. 10.1007/s100380170101
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Glycogen storage disease type Ia: molecular study in Brazilian patients.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 146, doi. 10.1007/s100380170102
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Four single-nucleotide polymorphisms in the human BUB1 gene.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 150, doi. 10.1007/PL00010920
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A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 152, doi. 10.1007/s100380170104
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Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genes.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 155, doi. 10.1007/s100380170105
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Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 158, doi. 10.1007/s100380170106
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Guidelines for genetic testing.
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- Journal of Human Genetics, 2001, v. 46, n. 3, p. 163, doi. 10.1007/s100380170107
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