000 | 01556 a2200469 4500 | ||
---|---|---|---|
005 | 20250513091742.0 | ||
264 | 0 | _c19961213 | |
008 | 199612s 0 0 eng d | ||
022 | _a0888-7543 | ||
024 | 7 |
_a10.1006/geno.1996.0237 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aRobinson, W P | |
245 | 0 | 0 |
_aDelineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion. _h[electronic resource] |
260 |
_bGenomics _cMay 1996 |
||
300 |
_a17-23 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aChromosome Mapping |
650 | 0 | 4 | _aChromosomes, Human, Pair 7 |
650 | 0 | 4 | _aDatabases, Factual |
650 | 0 | 4 |
_aElastin _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenetic Markers |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aPolymerase Chain Reaction |
650 | 0 | 4 | _aPolymorphism, Genetic |
650 | 0 | 4 | _aRepetitive Sequences, Nucleic Acid |
650 | 0 | 4 | _aSequence Deletion |
650 | 0 | 4 | _aSequence Homology, Nucleic Acid |
650 | 0 | 4 |
_aWilliams Syndrome _xgenetics |
700 | 1 | _aWaslynka, J | |
700 | 1 | _aBernasconi, F | |
700 | 1 | _aWang, M | |
700 | 1 | _aClark, S | |
700 | 1 | _aKotzot, D | |
700 | 1 | _aSchinzel, A | |
773 | 0 |
_tGenomics _gvol. 34 _gno. 1 _gp. 17-23 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1006/geno.1996.0237 _zAvailable from publisher's website |
999 |
_c8659915 _d8659915 |