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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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aCGH study for cryptic quantitative genomic imbalances Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 90 | 24 |
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Bone marrow culture for cancer Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 4 | 24 |
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Chromosome breakage study for Fanconi anemia Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 24 |
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Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 4 | 5 |
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Chromosome study from Amniotic fluid and CVS Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 6 | 24 |
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Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 7 | 23 |
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Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 2 |
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FISH study in Abortus(chromosome 13,16,18,21,X and Y) Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 4 | 6 |
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Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 2 | 2 |
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FISH study in Amniotic Fluid(Chromosome 13,18,21,X,Y) Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 3 | 5 |
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15q duplication study for autism Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Micro-deletion study for Miller-Dieker Lissencephaly Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Micro-deletion study for Wolf-Hirschhorn syndrome Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Micro-deletion study for Angelman syndrome Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Micro-deletion study for Prader-Willi syndrome Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Micro-deletion study for DiGeorge syndrome Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Hemoglobin E disease: Cd26(T-C) mutation study Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Hemoglobin D disease: Cd121G>C mutation study Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
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