-
1
-
-
0034611791
-
Obesity as a medical problem
-
Kopelman P.G. Obesity as a medical problem. Nature 2000, 404:635-643.
-
(2000)
Nature
, vol.404
, pp. 635-643
-
-
Kopelman, P.G.1
-
2
-
-
0037139451
-
Epidemic of obesity expands its spread to developing countries
-
Friedrich M.J. Epidemic of obesity expands its spread to developing countries. JAMA 2002, 287:1382-1386.
-
(2002)
JAMA
, vol.287
, pp. 1382-1386
-
-
Friedrich, M.J.1
-
3
-
-
84903135675
-
Centers for Disease Control and Prevention
-
Retrieved from
-
Centers for Disease Control and Prevention. National Health and Nutrition Examination Survey, 2006. Retrieved from. http://www.cdc.gov/nchs/nhanes.htm.
-
(2006)
National Health and Nutrition Examination Survey.
-
-
-
4
-
-
0035758099
-
Genetics of pathways regulating body weight in the development of obesity in humans
-
Froguel P., Boutin P. Genetics of pathways regulating body weight in the development of obesity in humans. Exp Biol Med 2001, 226:991-996.
-
(2001)
Exp Biol Med
, vol.226
, pp. 991-996
-
-
Froguel, P.1
Boutin, P.2
-
5
-
-
84900376109
-
Overweight and obesity. Kliegman: Nelson Textbook of Pediatrics
-
18th ed.
-
Joseph A, Skelton Colin D, Rudolph. Overweight and obesity. Kliegman: Nelson Textbook of Pediatrics, 18th ed. 2007; vol. 1(44).
-
(2007)
, vol.1
, pp. 44
-
-
Joseph, A.1
Skelton Colin, D.R.2
-
6
-
-
0033646938
-
Trends in the prevalence of obesity in children and adolescents in France between 1980 and 1991
-
Maillard G., Charles M.A., Tibult N. Trends in the prevalence of obesity in children and adolescents in France between 1980 and 1991. Int J Obes 2000, 24:1608-1617.
-
(2000)
Int J Obes
, vol.24
, pp. 1608-1617
-
-
Maillard, G.1
Charles, M.A.2
Tibult, N.3
-
7
-
-
0042831307
-
Minireview: human obesity-lessons from monogenic disorders
-
Stephen O'Rahilly I., Sadaf Farooqi, Giles S., Yeo H., Challis Benjamin G. Minireview: human obesity-lessons from monogenic disorders. Endocrinology 2003, 144(9):3757-3764.
-
(2003)
Endocrinology
, vol.144
, Issue.9
, pp. 3757-3764
-
-
Stephen O'Rahilly, I.1
Sadaf, F.2
Giles, S.3
Yeo, H.4
Challis Benjamin, G.5
-
9
-
-
0025293894
-
The body-mass index of twins who have been reared apart
-
Stunkard A.J., Harris J.R., Pedersen N.L., McClearn G.E. The body-mass index of twins who have been reared apart. N Engl J Med 1990, 322:1483-1487.
-
(1990)
N Engl J Med
, vol.322
, pp. 1483-1487
-
-
Stunkard, A.J.1
Harris, J.R.2
Pedersen, N.L.3
McClearn, G.E.4
-
10
-
-
0030843960
-
Genetic and environmental factors in relative body weight and human adiposity
-
Maes H.H., Neale M.C., Eaves L.J. Genetic and environmental factors in relative body weight and human adiposity. Behav Genet 1997, 27:325-351.
-
(1997)
Behav Genet
, vol.27
, pp. 325-351
-
-
Maes, H.H.1
Neale, M.C.2
Eaves, L.J.3
-
11
-
-
36048948343
-
Estudios sobre obesidad de origen monoge ́nico en humanos
-
Zurbano R., Ochoa M.C., Moreno-Aliaga M.J., Marti A. Estudios sobre obesidad de origen monoge ́nico en humanos. Revista Espan ̃ola de Obesidad 2004, 2:269-278.
-
(2004)
Revista Espan ̃ola de Obesidad
, vol.2
, pp. 269-278
-
-
Zurbano, R.1
Ochoa, M.C.2
Moreno-Aliaga, M.J.3
Marti, A.4
-
12
-
-
24644501291
-
Genetic and hereditary aspects of childhood obesity
-
Farooqi I.S. Genetic and hereditary aspects of childhood obesity. Best Pract Res Clin Endocrinol Metab 2005, 19:359-374.
-
(2005)
Best Pract Res Clin Endocrinol Metab
, vol.19
, pp. 359-374
-
-
Farooqi, I.S.1
-
13
-
-
33646410426
-
MC4R mutations-weight before screening!
-
Kublaoui B.M., Zinn A.R. MC4R mutations-weight before screening!. J Clin Endocrinol Metab 2006, 91:1671-1672.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1671-1672
-
-
Kublaoui, B.M.1
Zinn, A.R.2
-
14
-
-
33646404622
-
Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eating
-
Lubrano-Berthelier C., Dubern B., Lacorte J.M., Picard F., Shapiro A., Zhang S., et al. Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eating. J Clin Endocrinol Metab 2006, 91:1811-1818.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1811-1818
-
-
Lubrano-Berthelier, C.1
Dubern, B.2
Lacorte, J.M.3
Picard, F.4
Shapiro, A.5
Zhang, S.6
-
15
-
-
33749141489
-
Polymorphisms in the NPY and AGRP genes and body fatness in Dutch adults
-
Van Rossum C.T., Pijl H., Adan R.A., Hoebee B., Seidell J.C. Polymorphisms in the NPY and AGRP genes and body fatness in Dutch adults. Int J Obes (London) 2006, 30:1522-1528.
-
(2006)
Int J Obes (London)
, vol.30
, pp. 1522-1528
-
-
Van Rossum, C.T.1
Pijl, H.2
Adan, R.A.3
Hoebee, B.4
Seidell, J.C.5
-
16
-
-
33644658516
-
Ghrelin receptor mutations - too little height and too much hunger
-
Holst B., Schwartz T.W. Ghrelin receptor mutations - too little height and too much hunger. J Clin Invest 2006, 116:637-641.
-
(2006)
J Clin Invest
, vol.116
, pp. 637-641
-
-
Holst, B.1
Schwartz, T.W.2
-
17
-
-
29244451046
-
Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence
-
Hinrichs A.L., Wang J.C., Bufe B., Kwon J.M., Budde J., Allen R., et al. Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence. Am J Hum Genet 2006, 78:103-111.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 103-111
-
-
Hinrichs, A.L.1
Wang, J.C.2
Bufe, B.3
Kwon, J.M.4
Budde, J.5
Allen, R.6
-
18
-
-
0037458815
-
Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide
-
Kim U.K., Jorgenson E., Coon H., Leppert M., Risch N., Drayna D. Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science 2003, 299:1221-1225.
-
(2003)
Science
, vol.299
, pp. 1221-1225
-
-
Kim, U.K.1
Jorgenson, E.2
Coon, H.3
Leppert, M.4
Risch, N.5
Drayna, D.6
-
19
-
-
0036865752
-
Gln27Glu polymorphism in the beta2 adrenergic receptor gene and lipid metabolism during exercise in obese women
-
Macho-Azcarate T., Marti A., Gonzalez A., Martinez J.A., Ibanez J. Gln27Glu polymorphism in the beta2 adrenergic receptor gene and lipid metabolism during exercise in obese women. Int J Obes Relat Metab Disord 2002, 26:1434-1441.
-
(2002)
Int J Obes Relat Metab Disord
, vol.26
, pp. 1434-1441
-
-
Macho-Azcarate, T.1
Marti, A.2
Gonzalez, A.3
Martinez, J.A.4
Ibanez, J.5
-
20
-
-
0036592176
-
A maximal effort trial in obese women carrying the beta2- adrenoceptor Gln27Glu polymorphism
-
Macho-Azcarate T., Calabuig J., Marti A., Marti{dotless} ́nez J.A. A maximal effort trial in obese women carrying the beta2- adrenoceptor Gln27Glu polymorphism. J Physiol Biochem 2002, 58:103-108.
-
(2002)
J Physiol Biochem
, vol.58
, pp. 103-108
-
-
Macho-Azcarate, T.1
Calabuig, J.2
Marti, A.3
Marti ́ nez, J.A.4
-
21
-
-
0036525939
-
The 27Glu polymorphism of the beta2-adrenergic receptor interacts with physical activity influencing obesity risk among female subjects
-
Corbala ́n M.S., Marti A., Forga L., Martinez-Gonzalez M.A., Martinez J.A. The 27Glu polymorphism of the beta2-adrenergic receptor interacts with physical activity influencing obesity risk among female subjects. Clin Genet 2002, 61:305-307.
-
(2002)
Clin Genet
, vol.61
, pp. 305-307
-
-
Corbala ́ n, M.S.1
Marti, A.2
Forga, L.3
Martinez-Gonzalez, M.A.4
Martinez, J.A.5
-
22
-
-
0036933121
-
Beta(2)-Adrenergic receptor mutation and abdominal obesity risk: effect modification by gender and HDL-cholesterol
-
Corbalan M.S., Marti A., Forga L., Martinez-Gonzalez M.A., Martinez J.A. Beta(2)-Adrenergic receptor mutation and abdominal obesity risk: effect modification by gender and HDL-cholesterol. Eur J Nutr 2002, 41:114-118.
-
(2002)
Eur J Nutr
, vol.41
, pp. 114-118
-
-
Corbalan, M.S.1
Marti, A.2
Forga, L.3
Martinez-Gonzalez, M.A.4
Martinez, J.A.5
-
23
-
-
0036847664
-
TRP64ARG polymorphism of the beta3-adrenergic receptor gene and obesity risk: effect modification by a sedentary lifestyle
-
Marti A., Corbalan M.S., Martinez-Gonzalez M.A., Martinez J.A. TRP64ARG polymorphism of the beta3-adrenergic receptor gene and obesity risk: effect modification by a sedentary lifestyle. Diabetes Obes Metab 2002, 4:428-430.
-
(2002)
Diabetes Obes Metab
, vol.4
, pp. 428-430
-
-
Marti, A.1
Corbalan, M.S.2
Martinez-Gonzalez, M.A.3
Martinez, J.A.4
-
24
-
-
33846615902
-
Genetics of obesity: gene3diet interaction
-
Marti A., Martinez J.A. Genetics of obesity: gene3diet interaction. Int J Vitam Nutr Res 2006, 76:184-193.
-
(2006)
Int J Vitam Nutr Res
, vol.76
, pp. 184-193
-
-
Marti, A.1
Martinez, J.A.2
-
25
-
-
9444288703
-
Gene-gene interaction between PPARG2 and ADR beta 3 increases obesity risk in children
-
Grupo de Estudio Navarro de Obesidad Infantil (GENOI)
-
Ochoa M.C., Marti A., Azcona C., Chueca M., Oyarzabal M., et al. Gene-gene interaction between PPARG2 and ADR beta 3 increases obesity risk in children. Int J Obes Relat Metab Disord 2004, 28(Suppl. 3):S37-41. Grupo de Estudio Navarro de Obesidad Infantil (GENOI).
-
(2004)
Int J Obes Relat Metab Disord
, vol.28
, Issue.SUPPL. 3
-
-
Ochoa, M.C.1
Marti, A.2
Azcona, C.3
Chueca, M.4
Oyarzabal, M.5
-
27
-
-
23944444280
-
Single nucleotide variants in the beta2-adrenergic and beta3-adrenergic receptor genes explained 18.3% of adolescent obesity variation
-
Park H.S., Kim Y., Lee C. Single nucleotide variants in the beta2-adrenergic and beta3-adrenergic receptor genes explained 18.3% of adolescent obesity variation. J Hum Genet 2005, 50:365-369.
-
(2005)
J Hum Genet
, vol.50
, pp. 365-369
-
-
Park, H.S.1
Kim, Y.2
Lee, C.3
-
28
-
-
33746578398
-
Influence of lipoprotein lipase gene Ser447Stop and beta(1)-adrenergic receptor gene Arg389Gly polymorphisms and their interaction on obesity from childhood to adulthood: the Bogalusa Heart Study
-
Li S., Chen W., Srinivasan S.R., Boerwinkle E., Berenson G.S. Influence of lipoprotein lipase gene Ser447Stop and beta(1)-adrenergic receptor gene Arg389Gly polymorphisms and their interaction on obesity from childhood to adulthood: the Bogalusa Heart Study. Int J Obes (London) 2006, 30(8):1183-1188.
-
(2006)
Int J Obes (London)
, vol.30
, Issue.8
, pp. 1183-1188
-
-
Li, S.1
Chen, W.2
Srinivasan, S.R.3
Boerwinkle, E.4
Berenson, G.S.5
-
29
-
-
17844374080
-
Beta1-Adrenoceptor gene polymorphism predicts long-term changes in body weight
-
Linne Y., Dahlman I., Hoffstedt J. beta1-Adrenoceptor gene polymorphism predicts long-term changes in body weight. Int J Obes (London) 2005, 29:458-462.
-
(2005)
Int J Obes (London)
, vol.29
, pp. 458-462
-
-
Linne, Y.1
Dahlman, I.2
Hoffstedt, J.3
-
30
-
-
33645979693
-
[Influence of the 2866G/A polymorphism of the UCP2 gene on an obese pediatric population]
-
Grupo de Estudio Navarro de la obesidad infantil
-
Zurbano R., Ochoa M.C., Moreno-Aliaga M.J., Martinez J.A., Marti A. [Influence of the 2866G/A polymorphism of the UCP2 gene on an obese pediatric population]. Nutr Hosp 2006, 21:52-56. Grupo de Estudio Navarro de la obesidad infantil.
-
(2006)
Nutr Hosp
, vol.21
, pp. 52-56
-
-
Zurbano, R.1
Ochoa, M.C.2
Moreno-Aliaga, M.J.3
Martinez, J.A.4
Marti, A.5
-
31
-
-
2542486426
-
Higher obesity risk associated with the exon-8 insertion of the UCP2 gene in a Spanish case-control study
-
Marti A., Corbalan M.S., Forga L., Martinez-Gonzalez M.A., Martinez J.A. Higher obesity risk associated with the exon-8 insertion of the UCP2 gene in a Spanish case-control study. Nutrition 2004, 20:498-501.
-
(2004)
Nutrition
, vol.20
, pp. 498-501
-
-
Marti, A.1
Corbalan, M.S.2
Forga, L.3
Martinez-Gonzalez, M.A.4
Martinez, J.A.5
-
32
-
-
23844463466
-
Association of UCP3 gene 255C.T polymorphism and obesity in a Spanish population
-
Alonso A., Marti A., Corbalan M.S., Martinez-Gonzalez M.A., Forga L., Martinez J.A. Association of UCP3 gene 255C.T polymorphism and obesity in a Spanish population. Ann Nutr Metab 2005, 49:183-188.
-
(2005)
Ann Nutr Metab
, vol.49
, pp. 183-188
-
-
Alonso, A.1
Marti, A.2
Corbalan, M.S.3
Martinez-Gonzalez, M.A.4
Forga, L.5
Martinez, J.A.6
-
33
-
-
0036996163
-
CHO intake alters obesity risk associated with Pro12Ala polymorphism of PPARgamma Gene
-
Marti A., Corbalan M.S., Martinez-Gonzalez M.A., Forga L., Martinez J.A. CHO intake alters obesity risk associated with Pro12Ala polymorphism of PPARgamma Gene. J Physiol Biochem 2002, 58:219-220.
-
(2002)
J Physiol Biochem
, vol.58
, pp. 219-220
-
-
Marti, A.1
Corbalan, M.S.2
Martinez-Gonzalez, M.A.3
Forga, L.4
Martinez, J.A.5
-
35
-
-
33646562887
-
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)
-
Chiang A.P., Beck J.S., Yen H.J., Tayeh M.K., Scheetz T.E., Swiderski R.E., et al. Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). Proc Natl Acad Sci USA 2006, 103:6287-6292.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 6287-6292
-
-
Chiang, A.P.1
Beck, J.S.2
Yen, H.J.3
Tayeh, M.K.4
Scheetz, T.E.5
Swiderski, R.E.6
-
36
-
-
18744393073
-
Mutations in PHF6 are associated with Borjeson-Forssman-Lehmann syndrome
-
Lower K.M., Turner G., Kerr B.A., et al. Mutations in PHF6 are associated with Borjeson-Forssman-Lehmann syndrome. Nat Genet 2002, 32:661-665.
-
(2002)
Nat Genet
, vol.32
, pp. 661-665
-
-
Lower, K.M.1
Turner, G.2
Kerr, B.A.3
-
37
-
-
0015831045
-
A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies
-
Cohen M.M., Hall B.D., Smith D.W., et al. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr 1973, 83:280-284.
-
(1973)
J Pediatr
, vol.83
, pp. 280-284
-
-
Cohen, M.M.1
Hall, B.D.2
Smith, D.W.3
-
38
-
-
0037374844
-
Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome
-
Chandler K.E., Kidd A., Al-Gazali L., et al. Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome. J Med Genet 2003, 40:233-241.
-
(2003)
J Med Genet
, vol.40
, pp. 233-241
-
-
Chandler, K.E.1
Kidd, A.2
Al-Gazali, L.3
-
39
-
-
0031596498
-
Alstrom syndrome. Report of 22 cases and literature review
-
Russell-Eggitt I.M., Clayton P.T., Coffey R., et al. Alstrom syndrome. Report of 22 cases and literature review. Ophthalmology 1998, 105:1274-1280.
-
(1998)
Ophthalmology
, vol.105
, pp. 1274-1280
-
-
Russell-Eggitt, I.M.1
Clayton, P.T.2
Coffey, R.3
-
40
-
-
0029664835
-
Natural history of Alstrom syndrome in early childhood: onset with dilated cardiomyopathy
-
Michaud J.L., Heon E., Guilbert F., et al. Natural history of Alstrom syndrome in early childhood: onset with dilated cardiomyopathy. J Pediatr 1996, 128:225-229.
-
(1996)
J Pediatr
, vol.128
, pp. 225-229
-
-
Michaud, J.L.1
Heon, E.2
Guilbert, F.3
-
41
-
-
0036578890
-
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alstrom syndrome
-
Collin G.B., Marshall J.D., Ikeda A., et al. Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alstrom syndrome. Nat Genet 2002, 31:74-78.
-
(2002)
Nat Genet
, vol.31
, pp. 74-78
-
-
Collin, G.B.1
Marshall, J.D.2
Ikeda, A.3
-
42
-
-
2342635196
-
The fragile-X premutation: a maturing perspective
-
Hagerman P.J., Hagerman R.J. The fragile-X premutation: a maturing perspective. Am J Hum Genet 2004, 74:805-816.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 805-816
-
-
Hagerman, P.J.1
Hagerman, R.J.2
-
43
-
-
0037333288
-
New insights into fragile X syndrome: from molecules to neurobehaviors
-
Jin P., Warren S.T. New insights into fragile X syndrome: from molecules to neurobehaviors. Trends Biochem Sci 2003, 28:152-158.
-
(2003)
Trends Biochem Sci
, vol.28
, pp. 152-158
-
-
Jin, P.1
Warren, S.T.2
-
44
-
-
0030986873
-
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
-
Bamshad M., Lin R.C., Law D.J., Watkins W.C., Krakowiak P.A., Moore M.E., Franceschini P., Lala R., Holmes L.B., Gebuhr T.C., Bruneau B.G., Schinzel A., Seidman J.G., Seidman C.E., Jorde L.B. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Nat Genet 1997, 16:311-315.
-
(1997)
Nat Genet
, vol.16
, pp. 311-315
-
-
Bamshad, M.1
Lin, R.C.2
Law, D.J.3
Watkins, W.C.4
Krakowiak, P.A.5
Moore, M.E.6
Franceschini, P.7
Lala, R.8
Holmes, L.B.9
Gebuhr, T.C.10
Bruneau, B.G.11
Schinzel, A.12
Seidman, J.G.13
Seidman, C.E.14
Jorde, L.B.15
-
45
-
-
0033358672
-
Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome
-
Brzustowicz L.M.F.S., Khan M.B., Weksberg R. Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome. Am J Hum Genet 1999, 65:779-783.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 779-783
-
-
Brzustowicz, L.M.F.S.1
Khan, M.B.2
Weksberg, R.3
-
46
-
-
0025826768
-
New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255
-
Wilson M., Mulley J., Gedeon A., Robinson H., Turner G. New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255. Am J Med Genet 1991, 40:406-413.
-
(1991)
Am J Med Genet
, vol.40
, pp. 406-413
-
-
Wilson, M.1
Mulley, J.2
Gedeon, A.3
Robinson, H.4
Turner, G.5
-
47
-
-
85047698029
-
MEHMO (mental retardation, epileptic seizures, hypogenitalism, microcephaly, obesity): a new X-linked mitochondrial disorder
-
Leshinsky-Silver E., Zinger A., Bibi C.N., Barash V., Sadeh M., Lev D., Sagie T.L. MEHMO (mental retardation, epileptic seizures, hypogenitalism, microcephaly, obesity): a new X-linked mitochondrial disorder. Eur J Hum Genet 2002, 10:226-230.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 226-230
-
-
Leshinsky-Silver, E.1
Zinger, A.2
Bibi, C.N.3
Barash, V.4
Sadeh, M.5
Lev, D.6
Sagie, T.L.7
-
48
-
-
1042267409
-
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment
-
Goldstone A.P. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment. Trends Endocrinol Metab 2004, 15:12-20.
-
(2004)
Trends Endocrinol Metab
, vol.15
, pp. 12-20
-
-
Goldstone, A.P.1
-
49
-
-
0035393437
-
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus
-
Michaud J.L., Boucher F., Melnyk A., et al. Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus. Hum Mol Genet 2001, 10:1465-1473.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1465-1473
-
-
Michaud, J.L.1
Boucher, F.2
Melnyk, A.3
-
50
-
-
18444412266
-
Deletion of the SIM1 gene [6q16.2] in a patient with a Prader-Willi-like phenotype
-
Faivre L., Cormier-Daire V., Lapierre J.M., et al. Deletion of the SIM1 gene [6q16.2] in a patient with a Prader-Willi-like phenotype. J Med Genet 2002, 39:594-596.
-
(2002)
J Med Genet
, vol.39
, pp. 594-596
-
-
Faivre, L.1
Cormier-Daire, V.2
Lapierre, J.M.3
-
51
-
-
0025092242
-
Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene
-
Rose E.A., Glaser T., Jones C., et al. Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene. Cell 1990, 60:495-508.
-
(1990)
Cell
, vol.60
, pp. 495-508
-
-
Rose, E.A.1
Glaser, T.2
Jones, C.3
-
52
-
-
0036134782
-
Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome [11][p12p14]
-
Gul D., Ogur G., Tunca Y., Ozcan O. Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome [11][p12p14]. Am J Med Genet 2002, 107:70-71.
-
(2002)
Am J Med Genet
, vol.107
, pp. 70-71
-
-
Gul, D.1
Ogur, G.2
Tunca, Y.3
Ozcan, O.4
|