Property:AnswerB

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Showing 20 pages using this property.
W
WBR0106 +
Pheochromocytoma  +
WBR0107 +
Autosomal dominant  +
WBR0108 +
''COL3A1''  +
WBR0109 +
''p53''  +
WBR0110 +
Lisinopril  +
WBR0111 +
Von-Willebrand's disease  +
WBR0112 +
Abnormal development of the 2nd and 3rd branchial pouches  +
WBR0113 +
Quantitative PCR with primers mapping to chromosome 8 and chromosome 14  +
WBR0114 +
Decreased LH and FSH levels with absence of Barr body  +
WBR0115 +
Enveloped single-stranded negative-sense RNA virus  +
WBR0116 +
HLA-A3  +
WBR0117 +
Fever  +
WBR0118 +
5'...ACA GCT TAC GCC ATT...3'  +
WBR0119 +
44,XXY  +
WBR0120 +
Potassium ion channel  +
WBR0121 +
Dominant negative mutation  +
WBR0122 +
Deletion of a paternal-derived allele; methylation of a maternal-derived allele on chromosome 14  +
WBR0123 +
Deletion of paternal-derived allele; methylation of maternal-derived allele on chromosome 14  +
WBR0124 +
Deficiency of glucocerebrosidase enzyme  +
WBR0125 +
Brachial artery  +
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