| 000 | 01601 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250512030832.0 | ||
| 264 | 0 | _c19851017 | |
| 008 | 198510s 0 0 eng d | ||
| 022 | _a0028-4793 | ||
| 024 | 7 |
_a10.1056/NEJM198510033131402 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAntonarakis, S E | |
| 245 | 0 | 0 |
_aHemophilia A. Detection of molecular defects and of carriers by DNA analysis. _h[electronic resource] |
| 260 |
_bThe New England journal of medicine _cOct 1985 |
||
| 300 |
_a842-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 | _aCloning, Molecular |
| 650 | 0 | 4 |
_aDNA _xgenetics |
| 650 | 0 | 4 | _aDNA Restriction Enzymes |
| 650 | 0 | 4 |
_aFactor VIII _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes |
| 650 | 0 | 4 |
_aGenetic Carrier Screening _xmethods |
| 650 | 0 | 4 |
_aHemophilia A _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPrenatal Diagnosis _xmethods |
| 700 | 1 | _aWaber, P G | |
| 700 | 1 | _aKittur, S D | |
| 700 | 1 | _aPatel, A S | |
| 700 | 1 | _aKazazian, H H | |
| 700 | 1 | _aMellis, M A | |
| 700 | 1 | _aCounts, R B | |
| 700 | 1 | _aStamatoyannopoulos, G | |
| 700 | 1 | _aBowie, E J | |
| 700 | 1 | _aFass, D N | |
| 773 | 0 |
_tThe New England journal of medicine _gvol. 313 _gno. 14 _gp. 842-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1056/NEJM198510033131402 _zAvailable from publisher's website |
| 999 |
_c2999704 _d2999704 |
||