000 01247 a2200397 4500
005 20250515195623.0
264 0 _c20100312
008 201003s 0 0 eng d
022 _a1532-432X
024 7 _a10.3109/03630260903332866
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aIbarra, Bertha
245 0 0 _aHB Fannin-Lubbock-I with a single GGC>GAC mutation at beta119(GH2)Gly-->Asp in a homozygous Mexican patient.
_h[electronic resource]
260 _bHemoglobin
_c2009
300 _a492-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aExons
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aHaplotypes
650 0 4 _aHemoglobins, Abnormal
_xgenetics
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMexico
650 0 4 _aPedigree
650 0 4 _aPoint Mutation
650 0 4 _abeta-Globins
_xgenetics
700 1 _aAizpuru, Edna
700 1 _aSánchez-López, J Yoaly
700 1 _aMorales, Karina R
700 1 _aPerea, Francisco J
700 1 _aRuiz-Reyes, Guillermo
773 0 _tHemoglobin
_gvol. 33
_gno. 6
_gp. 492-7
856 4 0 _uhttps://doi.org/10.3109/03630260903332866
_zAvailable from publisher's website
999 _c19341227
_d19341227