| 000 | 01713 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250513031641.0 | ||
| 264 | 0 | _c19950530 | |
| 008 | 199505s 0 0 eng d | ||
| 022 | _a1059-7794 | ||
| 024 | 7 |
_a10.1002/humu.1380050104 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBelsham, D D | |
| 245 | 0 | 0 |
_aLeu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred. _h[electronic resource] |
| 260 |
_bHuman mutation _c1995 |
||
| 300 |
_a28-33 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 |
_aAndrogen-Insensitivity Syndrome _xgenetics |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aDNA, Complementary _xgenetics |
| 650 | 0 | 4 | _aDeoxyribonuclease HpaII |
| 650 | 0 | 4 | _aDeoxyribonucleases, Type II Site-Specific |
| 650 | 0 | 4 |
_aEthnicity _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Carrier Screening |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aManitoba |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 650 | 0 | 4 | _aPolymorphism, Restriction Fragment Length |
| 650 | 0 | 4 |
_aReceptors, Androgen _xgenetics |
| 650 | 0 | 4 | _aTransfection |
| 650 | 0 | 4 | _aX Chromosome |
| 700 | 1 | _aPereira, F | |
| 700 | 1 | _aGreenberg, C R | |
| 700 | 1 | _aLiao, S | |
| 700 | 1 | _aWrogemann, K | |
| 773 | 0 |
_tHuman mutation _gvol. 5 _gno. 1 _gp. 28-33 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.1380050104 _zAvailable from publisher's website |
| 999 |
_c7536605 _d7536605 |
||