000 | 01849 a2200613 4500 | ||
---|---|---|---|
005 | 20250515091620.0 | ||
264 | 0 | _c20080206 | |
008 | 200802s 0 0 eng d | ||
022 | _a1098-1004 | ||
024 | 7 |
_a10.1002/humu.20623 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aCallewaert, B L | |
245 | 0 | 0 |
_aArterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families. _h[electronic resource] |
260 |
_bHuman mutation _cJan 2008 |
||
300 |
_a150-8 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aArteries _xabnormalities |
650 | 0 | 4 |
_aConnective Tissue Diseases _xdiagnosis |
650 | 0 | 4 | _aFamily |
650 | 0 | 4 |
_aGlucose _xmetabolism |
650 | 0 | 4 | _aGlucose Tolerance Test |
650 | 0 | 4 |
_aGlucose Transport Proteins, Facilitative _xgenetics |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMagnetic Resonance Angiography |
650 | 0 | 4 | _aModels, Biological |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aSyndrome |
700 | 1 | _aWillaert, A | |
700 | 1 | _aKerstjens-Frederikse, W S | |
700 | 1 | _aDe Backer, J | |
700 | 1 | _aDevriendt, K | |
700 | 1 | _aAlbrecht, B | |
700 | 1 | _aRamos-Arroyo, M A | |
700 | 1 | _aDoco-Fenzy, M | |
700 | 1 | _aHennekam, R C M | |
700 | 1 | _aPyeritz, R E | |
700 | 1 | _aKrogmann, O N | |
700 | 1 | _aGillessen-kaesbach, G | |
700 | 1 | _aWakeling, E L | |
700 | 1 | _aNik-zainal, S | |
700 | 1 | _aFrancannet, C | |
700 | 1 | _aMauran, P | |
700 | 1 | _aBooth, C | |
700 | 1 | _aBarrow, M | |
700 | 1 | _aDekens, R | |
700 | 1 | _aLoeys, B L | |
700 | 1 | _aCoucke, P J | |
700 | 1 | _aDe Paepe, A M | |
773 | 0 |
_tHuman mutation _gvol. 29 _gno. 1 _gp. 150-8 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.20623 _zAvailable from publisher's website |
999 |
_c17455799 _d17455799 |