000 01331 a2200397 4500
005 20250513143150.0
264 0 _c19980723
008 199807s 0 0 eng d
022 _a0065-2598
024 7 _a10.1007/978-1-4615-5381-6_41
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aYamada, Y
245 0 0 _aPrenatal diagnosis of HPRT mutant genes in Lesch-Nyhan syndrome.
_h[electronic resource]
260 _bAdvances in experimental medicine and biology
_c1998
300 _a211-4 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aExons
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHumans
650 0 4 _aHypoxanthine Phosphoribosyltransferase
_xgenetics
650 0 4 _aIntrons
650 0 4 _aLesch-Nyhan Syndrome
_xdiagnosis
650 0 4 _aMale
650 0 4 _aPoint Mutation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
700 1 _aGoto, H
700 1 _aSuzumori, K
700 1 _aOgasawara, N
773 0 _tAdvances in experimental medicine and biology
_gvol. 431
_gp. 211-4
856 4 0 _uhttps://doi.org/10.1007/978-1-4615-5381-6_41
_zAvailable from publisher's website
999 _c9564791
_d9564791