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