Property:AnswerD

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Showing 20 pages using this property.
W
WBR0105 +
Mutation of ''HFE''  +
WBR0106 +
Parathyroid adenoma  +
WBR0107 +
X-linked dominant  +
WBR0108 +
''FBN1''  +
WBR0109 +
''PTEN''  +
WBR0110 +
Spironolactone  +
WBR0111 +
Factor VIII deficiency  +
WBR0112 +
Abnormal development of the branchial pouch responsible for the development of the thymus only  +
WBR0113 +
Northern Blot for fusion gene with probes mapping to chromosome 22 and chromosome 9  +
WBR0114 +
Decreased estrogen levels with a renal fusion anomaly  +
WBR0115 +
Non-enveloped single-stranded negative-sense RNA virus  +
WBR0116 +
HLA-DR5  +
WBR0117 +
Seizure  +
WBR0118 +
5'...ACA CAT TCC AAT ATC...3'  +
WBR0119 +
46,XX/XY  +
WBR0120 +
Ryanodine receptor  +
WBR0121 +
Haploinsufficiency  +
WBR0122 +
Deletion of a paternal-derived allele; methylation of a maternal-derived allele on chromosome 15  +
WBR0123 +
Deletion of paternal-derived allele; methylation of maternal-derived allele on chromosome 15  +
WBR0124 +
Deficiency of alpha-galactosidase A enzyme  +
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