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MUTATIONS IN THE RET PROTOONCOGENE ARE ASSOCIATED WITH MEN2A AND FMTC
DONIS KELLER H. | DOU S.
HUMAN MOLECULAR GENETICS
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FAMILIES OF MTDNA REARRANGEMENT CAN BE DETECTED IN PATIENTS WITH MTDNA DELETIONS: DUPLICATIONS MAY BE A TRANSIENT INTERMEDIATE FORM
POULTON J. | DEADMAN M.E. | BINDOFF L. | MORTEN K. | LAND J. | BROWN G.
View 156
GENOMIC ORGANIZATION OF THE SEQUENCE CODING FOR FIBRILLIN, THE DEFECTIVE GENE PRODUCT IN MARFAN SYNDROME
PEREIRA L. | D ALESSIO M. | RAMIREZ F. | SYKES B. | PANGILINAN T. | BONADIO J.
View 118