-
1
-
-
78651048074
-
Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins
-
Silver HK, Kiyasu W, George J, Deamer WC. Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins. Pediatrics 1953;12:368-76.
-
(1953)
Pediatrics
, vol.12
, pp. 368-376
-
-
Silver, H.K.1
Kiyasu, W.2
George, J.3
Deamer, W.C.4
-
2
-
-
0000771975
-
A syndrome of intra-uterine dwarfism recognizable at birth with craniofacial dysostosis, disproportionately short arms, and other anomalies (5 examples)
-
Russell A. A syndrome of intra-uterine dwarfism recognizable at birth with craniofacial dysostosis, disproportionately short arms, and other anomalies (5 examples). Proc R Soc Med 1954;47:1040-4.
-
(1954)
Proc R Soc Med
, vol.47
, pp. 1040-1044
-
-
Russell, A.1
-
3
-
-
0028827636
-
Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients
-
Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MB. Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients. Eur J Pediatr 1995;154:958-68.
-
(1995)
Eur J Pediatr
, vol.154
, pp. 958-968
-
-
Wollmann, H.A.1
Kirchner, T.2
Enders, H.3
Preece, M.A.4
Ranke, M.B.5
-
4
-
-
0032758850
-
The spectrum of Silver-Russell syndrome: A clinical and molecular genetic study and new diagnostic criteria
-
Price SM, Stanhope R, Garrett C, Preece MA, Trembath RC. The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 1999;36:837-42.
-
(1999)
J Med Genet
, vol.36
, pp. 837-842
-
-
Price, S.M.1
Stanhope, R.2
Garrett, C.3
Preece, M.A.4
Trembath, R.C.5
-
5
-
-
0028914364
-
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
-
Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie IW, Ilyina H, Méhes K, Hamel BCJ, Otten BJ, Hergersberg M, Werder E, Schoenle E, Schinzel A. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Hum Mol Genet 1995;4:583-7.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 583-587
-
-
Kotzot, D.1
Schmitt, S.2
Bernasconi, F.3
Robinson, W.P.4
Lurie, I.W.5
Ilyina, H.6
Méhes, K.7
Hamel, B.C.J.8
Otten, B.J.9
Hergersberg, M.10
Werder, E.11
Schoenle, E.12
Schinzel, A.13
-
6
-
-
42049087364
-
The genetic aetiology of Silver-Russell syndrome
-
Abu-Amero S, Monk D, Frost J, Preece M, Stanier P, Moore GE. The genetic aetiology of Silver-Russell syndrome. J Med Genet 2008;45:193-9.
-
(2008)
J Med Genet
, vol.45
, pp. 193-199
-
-
Abu-Amero, S.1
Monk, D.2
Frost, J.3
Preece, M.4
Stanier, P.5
Moore, G.E.6
-
7
-
-
77949769087
-
Epigenetic signatures of Silver-Russell syndrome
-
Abu-Amero S, Wakeling EL, Preece M, Whittaker J, Stanier P, Moore GE. Epigenetic signatures of Silver-Russell syndrome. J Med Genet 2010;47:150-4.
-
(2010)
J Med Genet
, vol.47
, pp. 150-154
-
-
Abu-Amero, S.1
Wakeling, E.L.2
Preece, M.3
Whittaker, J.4
Stanier, P.5
Moore, G.E.6
-
8
-
-
0036765999
-
Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation
-
Fisher AM, Thomas NS, Cockwell A, Stecko O, Kerr B, Temple IK, Clayton P. Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation. Hum Genet 2002;111:290-6.
-
(2002)
Hum Genet
, vol.111
, pp. 290-296
-
-
Fisher, A.M.1
Thomas, N.S.2
Cockwell, A.3
Stecko, O.4
Kerr, B.5
Temple, I.K.6
Clayton, P.7
-
9
-
-
30644459349
-
Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
-
Eggermann T, Meyer E, Obernann C, Heil I, Schüler H, Ranke MB, Eggermann K, Wollmann HA. Is maternal duplication of 11p15 associated with Silver-Russell syndrome? J Med Genet 2005;42:e26.
-
(2005)
J Med Genet
, vol.42
-
-
Eggermann, T.1
Meyer, E.2
Obernann, C.3
Heil, I.4
Schüler, H.5
Ranke, M.B.6
Eggermann, K.7
Wollmann, H.A.8
-
10
-
-
25144454048
-
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome
-
Gicquel C, Rossignol S, Cabrol S, Houang M, Steunou V, Barbu V, Danton F, Thibaud N, Le Merrer M, Burglen L, Bertrand A-M, Netchine I, Le Bouc Y. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nat Genet 2005;37:1003-7.
-
(2005)
Nat Genet
, vol.37
, pp. 1003-1007
-
-
Gicquel, C.1
Rossignol, S.2
Cabrol, S.3
Houang, M.4
Steunou, V.5
Barbu, V.6
Danton, F.7
Thibaud, N.8
Le Merrer, M.9
Burglen, L.10
Bertrand, A.-M.11
Netchine, I.12
Le Bouc, Y.13
-
11
-
-
34547764390
-
11p15 Imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: Clinical scoring system and epigenetic-phenotypic correlations
-
Netchine I, Rossignol S, Dufourg MN, Azzi S, Rousseau A, Perin L, Houang M, Steunou V, Esteva B, Thibaud N, Demay MC, Danton F, Petriczko E, Bertrand AM, Heinrichs C, Carel JC, Loeuille GA, Pinto G, Jacquemont ML, Gicquel C, Cabrol S, Le Bouc Y. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations. J Clin Endocrinol Metab 2007;92:3148-54.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3148-3154
-
-
Netchine, I.1
Rossignol, S.2
Dufourg, M.N.3
Azzi, S.4
Rousseau, A.5
Perin, L.6
Houang, M.7
Steunou, V.8
Esteva, B.9
Thibaud, N.10
Demay, M.C.11
Danton, F.12
Petriczko, E.13
Bertrand, A.M.14
Heinrichs, C.15
Carel, J.C.16
Loeuille, G.A.17
Pinto, G.18
Jacquemont, M.L.19
Gicquel, C.20
Cabrol, S.21
Le Bouc, Y.22
more..
-
12
-
-
33846461696
-
The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome
-
Schönherr N, Meyer E, Roos A, Schmidt A, Wollmann HA, Eggermann T. The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome. J Med Genet 2007;44:59-63.
-
(2007)
J Med Genet
, vol.44
, pp. 59-63
-
-
Schönherr, N.1
Meyer, E.2
Roos, A.3
Schmidt, A.4
Wollmann, H.A.5
Eggermann, T.6
-
13
-
-
0035058522
-
Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?
-
Hannula K, Kere J, Pirinen S, Holmberg C, Lipsanen-Nyman M. Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype? J Med Genet 2001;38:273-8.
-
(2001)
J Med Genet
, vol.38
, pp. 273-278
-
-
Hannula, K.1
Kere, J.2
Pirinen, S.3
Holmberg, C.4
Lipsanen-Nyman, M.5
-
14
-
-
59749088105
-
Clinically distinct epigenetic subgroups in Silver-Russell syndrome: The degree of H19 hypomethylation associates with SRS phenotype severity and genital and skeletal anomalies
-
Bruce S, Hannula-Jouppi K, Peltonen J, Kere J, Lipsanen-Nyman M. Clinically distinct epigenetic subgroups in Silver-Russell syndrome: the degree of H19 hypomethylation associates with SRS phenotype severity and genital and skeletal anomalies. J Clin Endocrinol Metab 2008;94:579-87.
-
(2008)
J Clin Endocrinol Metab
, vol.94
, pp. 579-587
-
-
Bruce, S.1
Hannula-Jouppi, K.2
Peltonen, J.3
Kere, J.4
Lipsanen-Nyman, M.5
-
15
-
-
62149105139
-
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes
-
Bartholdi D, Krajewska-Walasek M, Ounap K, Gaspar H, Chrzanowska KH, Ilyana H, Kayserili H, Lurie IW, Schinzel A, Baumer A. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. J Med Genet 2009;46:192-7.
-
(2009)
J Med Genet
, vol.46
, pp. 192-197
-
-
Bartholdi, D.1
Krajewska-Walasek, M.2
Ounap, K.3
Gaspar, H.4
Chrzanowska, K.H.5
Ilyana, H.6
Kayserili, H.7
Lurie, I.W.8
Schinzel, A.9
Baumer, A.10
-
16
-
-
50549093173
-
Maternal uniparental disomy 7 and Silver-Russell syndrome - Clinical update and comparison with other subgroups
-
Kotzot D. Maternal uniparental disomy 7 and Silver-Russell syndrome - clinical update and comparison with other subgroups. Eur J Med Genet 2008;51:444-51.
-
(2008)
Eur J Med Genet
, vol.51
, pp. 444-451
-
-
Kotzot, D.1
-
17
-
-
33645463808
-
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype
-
Bliek J, Terhal P, van den Bogaard MJ, Maas S, Hamel B, Salieb-Beugelaar G, Simon M, Letteboer T, van der Smagt J, Kroes H, Mannens M. Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype. Am J Hum Genet 2006;78:604-14.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 604-614
-
-
Bliek, J.1
Terhal, P.2
Van Den Bogaard, M.J.3
Maas, S.4
Hamel, B.5
Salieb-Beugelaar, G.6
Simon, M.7
Letteboer, T.8
Van Der Smagt, J.9
Kroes, H.10
Mannens, M.11
-
18
-
-
33749259925
-
(Epi) mutations in 11p15 significantly contribute to Silver-Russell syndrome: But are they generally involved in growth retardation?
-
Schönherr N, Meyer E, Eggermann K, Ranke MB, Wollmann HA, Eggermann T. (Epi) mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation? Eur J Med Genet 2006;49:414-18.
-
(2006)
Eur J Med Genet
, vol.49
, pp. 414-418
-
-
Schönherr, N.1
Meyer, E.2
Eggermann, K.3
Ranke, M.B.4
Wollmann, H.A.5
Eggermann, T.6
-
19
-
-
42049122139
-
The endocrine phenotype in Silver-Russell syndrome is defined by the underlying epigenetic alteration
-
Binder G, Seidel AK, Martin DD, Schweizer R, Schwarze CP, Wollmann HA, Eggermann T, Ranke M. The endocrine phenotype in Silver-Russell syndrome is defined by the underlying epigenetic alteration. J Clin Endocrinol Metab 2008;93:1402-7.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 1402-1407
-
-
Binder, G.1
Seidel, A.K.2
Martin, D.D.3
Schweizer, R.4
Schwarze, C.P.5
Wollmann, H.A.6
Eggermann, T.7
Ranke, M.8
-
20
-
-
39749173843
-
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia
-
Zeschnigk M, Albrecht B, Buiting K, Kanber D, Eggermann T, Binder G, Gromoll J, Prott E-C, Seland S, Horsthemke B. IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia. Eur J Hum Genet 2008;16:328-34.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 328-334
-
-
Zeschnigk, M.1
Albrecht, B.2
Buiting, K.3
Kanber, D.4
Eggermann, T.5
Binder, G.6
Gromoll, J.7
Prott, E.-C.8
Seland, S.9
Horsthemke, B.10
-
21
-
-
66049151670
-
Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation
-
Eggermann T, Gonzalez D, Spengler S, Arslan-Kirchner M, Binder G, Schönherr N. Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation. Pediatrics 2009;123:e929-31.
-
(2009)
Pediatrics
, vol.123
-
-
Eggermann, T.1
Gonzalez, D.2
Spengler, S.3
Arslan-Kirchner, M.4
Binder, G.5
Schönherr, N.6
-
22
-
-
39149142187
-
Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation
-
Scott RH, Douglas J, Baskcomb L, Nygren AO, Birch JM, Cole TR, Cormier-Daire V, Eastwood DM, Garcia-Minaur S, Lupunzina P, Tatton-Brown K, Bliek J, Maher E, Rahman N. Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation. J Med Genet 2008;45:106-13.
-
(2008)
J Med Genet
, vol.45
, pp. 106-113
-
-
Scott, R.H.1
Douglas, J.2
Baskcomb, L.3
Nygren, A.O.4
Birch, J.M.5
Cole, T.R.6
Cormier-Daire, V.7
Eastwood, D.M.8
Garcia-Minaur, S.9
Lupunzina, P.10
Tatton-Brown, K.11
Bliek, J.12
Maher, E.13
Rahman, N.14
-
23
-
-
62849117124
-
Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis
-
Alders M, Bliek J, vd Lip K, vd Bogaard R, Mannens M. Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis. Eur J Hum Genet 2009;17:467-73.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 467-473
-
-
Alders, M.1
Bliek, J.2
Vd Lip, K.3
Vd Bogaard, R.4
Mannens, M.5
-
24
-
-
67349253397
-
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome
-
Bliek J, Verde G, Callaway J, Maas S, De Crescenzo A, Sparago A, Cerrato F, Russo S, Ferraiuolo S, Rinaldi M, Fischetto R, Lalatta F, Giordano L, Ferrari P, Cubellis M, Larizza L, Temple IK, Mannens M, Mackay DJG, Riccio A. Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome. Eur J Hum Genet 2008;17:611-19.
-
(2008)
Eur J Hum Genet
, vol.17
, pp. 611-619
-
-
Bliek, J.1
Verde, G.2
Callaway, J.3
Maas, S.4
De Crescenzo, A.5
Sparago, A.6
Cerrato, F.7
Russo, S.8
Ferraiuolo, S.9
Rinaldi, M.10
Fischetto, R.11
Lalatta, F.12
Giordano, L.13
Ferrari, P.14
Cubellis, M.15
Larizza, L.16
Temple, I.K.17
Mannens, M.18
Mackay, D.J.G.19
Riccio, A.20
more..
-
25
-
-
45249092139
-
Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome
-
Bullman H, Lever M, Robinson DO, Mackay DJ, Holder SE, Wakeling EL. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome. J Med Genet 2008;45:396-9.
-
(2008)
J Med Genet
, vol.45
, pp. 396-399
-
-
Bullman, H.1
Lever, M.2
Robinson, D.O.3
Mackay, D.J.4
Holder, S.E.5
Wakeling, E.L.6
-
27
-
-
33751113031
-
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
-
Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet 2006;79:965-72.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 965-972
-
-
Feuk, L.1
Kalervo, A.2
Lipsanen-Nyman, M.3
Skaug, J.4
Nakabayashi, K.5
Finucane, B.6
Hartung, D.7
Innes, M.8
Kerem, B.9
Nowaczyk, M.J.10
Rivlin, J.11
Roberts, W.12
Senman, L.13
Summers, A.14
Szatmari, P.15
Wong, V.16
Vincent, J.B.17
Zeesman, S.18
Osborne, L.R.19
Cardy, J.O.20
Kere, J.21
Scherer, S.W.22
Hannula-Jouppi, K.23
more..
-
28
-
-
0037110930
-
Gastrointestinal complications of Russell-Silver syndrome: A pilot study
-
Anderson J, Viskochil D, O'Gorman M, Gonzales C. Gastrointestinal complications of Russell-Silver syndrome: a pilot study. Am J Med Genet 2002;113:15-19.
-
(2002)
Am J Med Genet
, vol.113
, pp. 15-19
-
-
Anderson, J.1
Viskochil, D.2
O'Gorman, M.3
Gonzales, C.4
-
29
-
-
54049098434
-
Myoclonus-dystonia due to maternal uniparental disomy
-
Guettard E, Portnoi M-F, Lohmann-Hedrich K, Keren B, Rossignol S, Winkler S, Kamel I, Leu S, Apartis E, Vidailhet Klein C, Roze E. Myoclonus-dystonia due to maternal uniparental disomy. Arch Neurol 2008;65:1380-5.
-
(2008)
Arch Neurol
, vol.65
, pp. 1380-1385
-
-
Guettard, E.1
Portnoi, M.-F.2
Lohmann-Hedrich, K.3
Keren, B.4
Rossignol, S.5
Winkler, S.6
Kamel, I.7
Leu, S.8
Apartis, E.9
Vidailhet Klein, C.10
Roze, E.11
-
30
-
-
67649499947
-
Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia
-
Carbon M, Niethammer M, Peng S, Raymond D, Dhawan V, Chaly T, Ma Y, Bressman S, Eidelberg D. Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia. Neurology 2009;72:2097-103.
-
(2009)
Neurology
, vol.72
, pp. 2097-2103
-
-
Carbon, M.1
Niethammer, M.2
Peng, S.3
Raymond, D.4
Dhawan, V.5
Chaly, T.6
Ma, Y.7
Bressman, S.8
Eidelberg, D.9
-
31
-
-
0034530186
-
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
-
Engel J, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome. J Med Genet 2000;37:921-6.
-
(2000)
J Med Genet
, vol.37
, pp. 921-926
-
-
Engel, J.1
Smallwood, A.2
Harper, A.3
Higgins, M.J.4
Oshimura, M.5
Reik, W.6
Schofield, P.N.7
Maher, E.R.8
-
32
-
-
70450162112
-
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
-
Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, Le Jule M, Heinrichs C, Cabrol S, Gicquel C, Le Bouc Y, Netchine I. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum Mol Genet 2009;18:4724-33.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4724-4733
-
-
Azzi, S.1
Rossignol, S.2
Steunou, V.3
Sas, T.4
Thibaud, N.5
Danton, F.6
Le Jule, M.7
Heinrichs, C.8
Cabrol, S.9
Gicquel, C.10
Le Bouc, Y.11
Netchine, I.12
-
33
-
-
17444391320
-
Imprinting and assisted reproductive technology
-
Maher ER. Imprinting and assisted reproductive technology. Hum Mol Genet 2005;14:133-8.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 133-138
-
-
Maher, E.R.1
-
34
-
-
23844480131
-
Increased risk of Silver-Russell syndrome after in vitro fertilization?
-
Svensson J, Bjornstahl A, Ivarsson SA. Increased risk of Silver-Russell syndrome after in vitro fertilization? Acta Paediatr 2005;94:1163-5.
-
(2005)
Acta Paediatr
, vol.94
, pp. 1163-1165
-
-
Svensson, J.1
Bjornstahl, A.2
Ivarsson, S.A.3
-
35
-
-
0037035121
-
Low and very low birth weight in infants conceived with use of assisted reproductive technology
-
Schieve LA, Meikle SF, Ferre C, Peterson HB, Jeng G, Wilcox LS. Low and very low birth weight in infants conceived with use of assisted reproductive technology. N Engl J Med 2002;346:731-7.
-
(2002)
N Engl J Med
, vol.346
, pp. 731-737
-
-
Schieve, L.A.1
Meikle, S.F.2
Ferre, C.3
Peterson, H.B.4
Jeng, G.5
Wilcox, L.S.6
-
36
-
-
34548081379
-
Infertility, assisted reproduction technologies and imprinting disturbances: A Dutch study
-
DOI 10.1093/humrep/dem172
-
Doornbos ME, Maas SM, McDonnell J, Vermeiden JP, Hennekam RC. Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study. Hum Reprod 2007;22:2476-80. (Pubitemid 47289064)
-
(2007)
Human Reproduction
, vol.22
, Issue.9
, pp. 2476-2480
-
-
Doornbos, M.E.1
Maas, S.M.2
McDonnell, J.3
Vermeiden, J.P.W.4
Hennekam, R.C.M.5
-
37
-
-
0026772772
-
Type 2 (non-insulin-dependent) diabetes mellitus: The thrifty phenotype hypothesis
-
Barker DJ, Hales CN. Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis. Diabetologia 1992;35:595-601.
-
(1992)
Diabetologia
, vol.35
, pp. 595-601
-
-
Barker, D.J.1
Hales, C.N.2
-
38
-
-
77955013374
-
Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients
-
Published Online First: Sep 14
-
Bruce S, Hannula-Jouppi K, Puoskari M, Fransson I, Simola KO, Lipsanen-Nyman M, Kere J. Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients. J Med Genet. Published Online First: 2009 Sep 14.
-
(2009)
J Med Genet
-
-
Bruce, S.1
Hannula-Jouppi, K.2
Puoskari, M.3
Fransson, I.4
Simola, K.O.5
Lipsanen-Nyman, M.6
Kere, J.7
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