000 | 00953 a2200301 4500 | ||
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005 | 20250513201542.0 | ||
264 | 0 | _c20000107 | |
008 | 200001s 0 0 eng d | ||
022 | _a0022-2593 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aTischkowitz, M | |
245 | 0 | 0 |
_aAmelogenesis imperfecta, sensorineural hearing loss, and Beau's lines, a second case report of Heimler's syndrome. _h[electronic resource] |
260 |
_bJournal of medical genetics _cDec 1999 |
||
300 |
_a941-3 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Letter | ||
650 | 0 | 4 |
_aAmelogenesis Imperfecta _xgenetics |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aHearing Loss, Sensorineural _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aSyndrome |
700 | 1 | _aClenaghan, C | |
700 | 1 | _aDavies, S | |
700 | 1 | _aHunter, L | |
700 | 1 | _aPotts, J | |
700 | 1 | _aVerhoef, S | |
773 | 0 |
_tJournal of medical genetics _gvol. 36 _gno. 12 _gp. 941-3 |
|
999 |
_c10592078 _d10592078 |