| 000 | 01556 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250514182533.0 | ||
| 264 | 0 | _c20040617 | |
| 008 | 200406s 0 0 eng d | ||
| 022 | _a0009-9163 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.2004.00227.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTabori, U | |
| 245 | 0 | 0 |
_aDetection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome. _h[electronic resource] |
| 260 |
_bClinical genetics _cApr 2004 |
||
| 300 |
_a322-6 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDNA-Binding Proteins _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHomeodomain Proteins _xgenetics |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aNuclear Proteins |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPrenatal Diagnosis _xmethods |
| 650 | 0 | 4 | _aReligion |
| 650 | 0 | 4 |
_aSevere Combined Immunodeficiency _xdiagnosis |
| 700 | 1 | _aMark, Z | |
| 700 | 1 | _aAmariglio, N | |
| 700 | 1 | _aEtzioni, A | |
| 700 | 1 | _aGolan, H | |
| 700 | 1 | _aBiloray, B | |
| 700 | 1 | _aToren, A | |
| 700 | 1 | _aRechavi, G | |
| 700 | 1 | _aDalal, I | |
| 773 | 0 |
_tClinical genetics _gvol. 65 _gno. 4 _gp. 322-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.2004.00227.x _zAvailable from publisher's website |
| 999 |
_c14743973 _d14743973 |
||