000 | 02055 a2200601 4500 | ||
---|---|---|---|
005 | 20250513051419.0 | ||
264 | 0 | _c19940718 | |
008 | 199407s 0 0 eng d | ||
022 | _a0964-6906 | ||
024 | 7 |
_a10.1093/hmg/3.2.237 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aEng, C | |
245 | 0 | 0 |
_aPoint mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. _h[electronic resource] |
260 |
_bHuman molecular genetics _cFeb 1994 |
||
300 |
_a237-41 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAdenoma _xgenetics |
650 | 0 | 4 |
_aAdrenal Gland Neoplasms _xgenetics |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 |
_aCarcinoma, Medullary _xgenetics |
650 | 0 | 4 | _aCodon |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aDNA, Neoplasm _xgenetics |
650 | 0 | 4 | _aDrosophila Proteins |
650 | 0 | 4 | _aExons |
650 | 0 | 4 |
_aHirschsprung Disease _xgenetics |
650 | 0 | 4 | _aHyperplasia |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 |
_aMultiple Endocrine Neoplasia _xgenetics |
650 | 0 | 4 |
_aParathyroid Glands _xpathology |
650 | 0 | 4 |
_aParathyroid Neoplasms _xgenetics |
650 | 0 | 4 |
_aPheochromocytoma _xgenetics |
650 | 0 | 4 | _aPoint Mutation |
650 | 0 | 4 | _aProtein Structure, Tertiary |
650 | 0 | 4 | _aProtein-Tyrosine Kinases |
650 | 0 | 4 |
_aProto-Oncogene Proteins _xchemistry |
650 | 0 | 4 | _aProto-Oncogene Proteins c-ret |
650 | 0 | 4 | _aProto-Oncogenes |
650 | 0 | 4 |
_aReceptor Protein-Tyrosine Kinases _xchemistry |
650 | 0 | 4 |
_aThyroid Neoplasms _xgenetics |
700 | 1 | _aSmith, D P | |
700 | 1 | _aMulligan, L M | |
700 | 1 | _aNagai, M A | |
700 | 1 | _aHealey, C S | |
700 | 1 | _aPonder, M A | |
700 | 1 | _aGardner, E | |
700 | 1 | _aScheumann, G F | |
700 | 1 | _aJackson, C E | |
700 | 1 | _aTunnacliffe, A | |
773 | 0 |
_tHuman molecular genetics _gvol. 3 _gno. 2 _gp. 237-41 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1093/hmg/3.2.237 _zAvailable from publisher's website |
999 |
_c7911033 _d7911033 |