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| genetics | 5 | 5 | 6 | |
| harlequin ichthyosis | 4 | 4 | 2 | |
| - | 2 | 2 | 4 | |
| codominance | 2 | 2 | 1 | |
| treacher collins syndrome | 2 | 3 | 7 | |
| patau | 2 | 2 | 3 | |
| alzheimers studies early onset | 1 | 1 | 2 | |
| porphyriacutaneatarda | 1 | 1 | 1 | |
| information on hemophilia | 1 | 1 | 4 | |
| chromosome 10 | 1 | 2 | 3 | |
| males with klinefelter syndrome | 1 | 1 | 1 | |
| triple x syndrome | 1 | 1 | 4 | |
| sensory nerves | 1 | 1 | 1 | |
| methylmalonic acidemia | 1 | 1 | 3 | |
| hereditary nonpolyposis colorectal cancer | 1 | 1 | 1 | |
| brca2 gene research | 1 | 1 | 1 | |
| hypothyroidism | 1 | 1 | 20 | |
| different type of genetics | 1 | 1 | 1 | |
| turnersyndrome | 1 | 1 | 4 | |
| brca gene | 1 | 1 | 5 | |
| huntington's disease | 1 | 1 | 16 | |
| astrocytes | 1 | 1 | 3 | |
| deafness and genetics | 1 | 1 | 1 | |
| factor v blood disorder information | 1 | 1 | 2 | |
| frameshift mutations | 1 | 2 | 2 | |
| lien | 1 | 1 | 8 | |
| progeria | 1 | 1 | 37 | |
| familial adenomatous polyposis | 1 | 1 | 3 | |
| gene deletion | 1 | 1 | 4 | |
| connection lobular cancer melanoma | 1 | 1 | 6 | |
| low gamma glutamyl transferase enzyme | 1 | 1 | 2 | |
| adenomatosis | 1 | 1 | 9 | |
| trace genetic disorders in my family | 1 | 2 | 4 | |
| muscle tone | 1 | 1 | 5 | |
| leiden factor v | 1 | 1 | 4 | |
| myalgia | 1 | 1 | 10 | |
| monosomy chromosome 22 | 1 | 1 | 1 | |
| y chromosomes | 1 | 1 | 1 | |
| medical help charcot marie tooth syndrome | 1 | 1 | 1 | |
| is alzheimer's disease a genetic disease | 1 | 1 | 3 | |
| chromosome 22 abnormalities | 1 | 1 | 1 | |
| what type of mutation is the genetic disorder achondroplasia | 1 | 1 | 8 | |
| porphyria cutanea tarda | 1 | 1 | 3 | |
| leiden factor 5 | 1 | 1 | 7 | |
| cowden syndrome | 1 | 1 | 1 | |
| what is androgen | 1 | 1 | 9 | |
| turner syndrome information | 1 | 1 | 3 | |
| chromosome 13 | 1 | 1 | 3 | |
| neuropathy | 1 | 1 | 40 | |
| homozygous | 1 | 1 | 9 | |
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