| 000 | 01322 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250511181119.0 | ||
| 264 | 0 | _c19920526 | |
| 008 | 199205s 0 0 eng d | ||
| 022 | _a0002-9297 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBiancalana, V | |
| 245 | 0 | 0 |
_aConfirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. _h[electronic resource] |
| 260 |
_bAmerican journal of human genetics _cMay 1992 |
||
| 300 |
_a981-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Linkage _xgenetics |
| 650 | 0 | 4 |
_aGenetic Markers _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPolymorphism, Restriction Fragment Length |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 | _aX Chromosome |
| 700 | 1 | _aBriard, M L | |
| 700 | 1 | _aDavid, A | |
| 700 | 1 | _aGilgenkrantz, S | |
| 700 | 1 | _aKaplan, J | |
| 700 | 1 | _aMathieu, M | |
| 700 | 1 | _aPiussan, C | |
| 700 | 1 | _aPoncin, J | |
| 700 | 1 | _aSchinzel, A | |
| 700 | 1 | _aOudet, C | |
| 773 | 0 |
_tAmerican journal of human genetics _gvol. 50 _gno. 5 _gp. 981-7 |
|
| 999 |
_c1355700 _d1355700 |
||