Citations for
1CPHD2, KAL1, LEPR, OBS1
The Molecular Basis of Human Hypogonadotropic Hypogonadism.
Layman LC.
Mol Genet Metab 68(2):191-199 1999
2LEP, OBS1
A leptin missense mutation associated with hypogonadism and morbid obesity.
Strobel A, Issad T, Camoin L, Ozata M, Strosberg AD.
Nat Genet 18(3):213-5. 1998
3OBS1, LEP
Markers for the gene ob and serum leptin levels in human morbid obesity.
Oksanen L, Ohman M, Heiman M, Kainulainen K, Kaprio J, Mustajoki P, Koivisto V, Koskenvuo M, Janne OA, Peltonen L, Kontula K.
Hum Genet 99(5):559-64. 1997
4LEP, OBS1
Congenital leptin deficiency is associated with severe early-onset obesity in humans.
Montague CT, Farooqi IS, Whitehead JP, Soos MA, Rau H, Wareham NJ, Sewter CP, Digby JE, Mohammed SN, Hurst JA, Cheetham CH, Earley AR, Barnett AH, Prins JB, O'Rahilly S.
Nature 387(6636):903-8. 1997
5LEP, OBS1
Indication for linkage of the human OB gene region with extreme obesity.
Clement K, et al.
Diabetes 45 : 687-690. 1996
6LEP, OBS1
Extreme obesity may be linked to markers flanking the human OB gene.
Reed DR, et al.
Diabetes 45 : 691-694. 1996
7OBS1, LEP
A novel microsatellite polymorphism in the human OB gene : a highly polymorphic marker for linkage analysis.
Shintani M, et al.
Diabetologia 39 : 1398-1401. 1996