-
1
-
-
0034758284
-
Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region
-
J.E. Whittington, A.J. Holland, T. Webb, J. Butler, D. Clarke, and H. Boer Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region J Med Genet 38 2001 792 798
-
(2001)
J Med Genet
, vol.38
, pp. 792-798
-
-
Whittington, J.E.1
Holland, A.J.2
Webb, T.3
Butler, J.4
Clarke, D.5
Boer, H.6
-
2
-
-
0021314588
-
Prader-Willi syndrome
-
S.B. Cassidy Prader-Willi syndrome Curr Probl Pediatr 14 1984 1 55
-
(1984)
Curr Probl Pediatr
, vol.14
, pp. 1-55
-
-
Cassidy, S.B.1
-
3
-
-
0027476242
-
Prader-Willi syndrome: Consensus diagnostic criteria
-
V.A. Holm, S.B. Cassidy, M.G. Butler, J.M. Hanchett, L.R. Greenswag, B.Y. Whitman, et al. Prader-Willi syndrome: Consensus diagnostic criteria Pediatrics 91 1993 398 402
-
(1993)
Pediatrics
, vol.91
, pp. 398-402
-
-
Holm, V.A.1
Cassidy, S.B.2
Butler, M.G.3
Hanchett, J.M.4
Greenswag, L.R.5
Whitman, B.Y.6
-
4
-
-
0026353331
-
Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients
-
W.P. Robinson, A. Bottani, Y.G. Xie, J. Balakrishman, F. Binkert, M. Machler, et al. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients Am J Hum Genet 49 1991 1219 1234
-
(1991)
Am J Hum Genet
, vol.49
, pp. 1219-1234
-
-
Robinson, W.P.1
Bottani, A.2
Xie, Y.G.3
Balakrishman, J.4
Binkert, F.5
Machler, M.6
-
5
-
-
0028900374
-
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome
-
G. Gillessen-Kaesbach, S. Gross, S. Kaya-Westerloh, E. Passarge, and B. Horsthemke DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome J Med Genet 32 1995 88 92
-
(1995)
J Med Genet
, vol.32
, pp. 88-92
-
-
Gillessen-Kaesbach, G.1
Gross, S.2
Kaya-Westerloh, S.3
Passarge, E.4
Horsthemke, B.5
-
6
-
-
0029874866
-
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)
-
M. Erdel, S. Schuffenhauer, B. Buchholz, U. Barth-Witte, S. Kochl, B. Utermann, et al. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10) Hum Genet 97 1996 784 793
-
(1996)
Hum Genet
, vol.97
, pp. 784-793
-
-
Erdel, M.1
Schuffenhauer, S.2
Buchholz, B.3
Barth-Witte, U.4
Kochl, S.5
Utermann, B.6
-
7
-
-
0035515362
-
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria
-
M. Gunay-Aygun, S. Schwartz, S. Heeger, M.A. O'Riordan, and S.B. Cassidy The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria Pediatrics 108 2001 E92
-
(2001)
Pediatrics
, vol.108
-
-
Gunay-Aygun, M.1
Schwartz, S.2
Heeger, S.3
O'Riordan, M.A.4
Cassidy, S.B.5
-
8
-
-
1442323876
-
Behavioral differences among subjects with Prader-Willi syndrome and type i or type ii deletion and maternal disomy
-
M.G. Butler, D.C. Bittel, N. Kibiryeva, Z. Talebizadeh, and T. Thompson Behavioral differences among subjects with Prader-Willi syndrome and type i or type ii deletion and maternal disomy Pediatrics 113 2004 565 573
-
(2004)
Pediatrics
, vol.113
, pp. 565-573
-
-
Butler, M.G.1
Bittel, D.C.2
Kibiryeva, N.3
Talebizadeh, Z.4
Thompson, T.5
-
9
-
-
0037447443
-
Genomnic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class ii (BP2/3) deletions
-
G. Gimelli, M.A. Pujana, M.G. Patricelli, S. Russo, D. Giardino, L. Larizza, et al. Genomnic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class ii (BP2/3) deletions Hum Mol Genet 12 2003 849 858
-
(2003)
Hum Mol Genet
, vol.12
, pp. 849-858
-
-
Gimelli, G.1
Pujana, M.A.2
Patricelli, M.G.3
Russo, S.4
Giardino, D.5
Larizza, L.6
-
10
-
-
0032971379
-
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)
-
S.L. Christian, J.A. Fantes, S.K. Mewborn, B. Huang, and D.H. Ledbetter Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13) Hum Mol Genet 8 1999 1025 1037
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1025-1037
-
-
Christian, S.L.1
Fantes, J.A.2
Mewborn, S.K.3
Huang, B.4
Ledbetter, D.H.5
-
11
-
-
0035136724
-
Molecular characterization of four cases of intrachromosomal triplication of chromosome 15q11-q14
-
P. Ungaro, S.L. Christian, J.A. Fantes, A. Mutirangura, S. Black, J. Reynolds, et al. Molecular characterization of four cases of intrachromosomal triplication of chromosome 15q11-q14 J Med Genet 38 2001 26 34
-
(2001)
J Med Genet
, vol.38
, pp. 26-34
-
-
Ungaro, P.1
Christian, S.L.2
Fantes, J.A.3
Mutirangura, A.4
Black, S.5
Reynolds, J.6
-
12
-
-
0026680691
-
Uniparental disomy 15 resulting from «correction» of an initial trisomy 15
-
S.G. Purvis-Smith, T. Saville, S. Manass, M.Y. Yip, P.R. Lam-Po-Tang, B. Duffy, et al. Uniparental disomy 15 resulting from «correction» of an initial trisomy 15 Am J Hum Genet 50 1992 1348 1350
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1348-1350
-
-
Purvis-Smith, S.G.1
Saville, T.2
Manass, S.3
Yip, M.Y.4
Lam-Po-Tang, P.R.5
Duffy, B.6
-
13
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
R.D. Nicholls, and J.L. Knepper Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes Annu Rev Genomics Hum Genet 2 2001 153 175
-
(2001)
Annu Rev Genomics Hum Genet
, vol.2
, pp. 153-175
-
-
Nicholls, R.D.1
Knepper, J.L.2
-
14
-
-
0037371674
-
Epimutations in Prader-Willi and Angelman syndromes: A molecular study of 136 patients with an imprinting defect
-
K. Buiting, S. Gross, C. Lich, G. Gillessen-Kaesbach, O. El-Maarri, and B. Horsthemke Epimutations in Prader-Willi and Angelman syndromes: A molecular study of 136 patients with an imprinting defect Am J Hum Genet 72 2003 571 577
-
(2003)
Am J Hum Genet
, vol.72
, pp. 571-577
-
-
Buiting, K.1
Gross, S.2
Lich, C.3
Gillessen-Kaesbach, G.4
El-Maarri, O.5
Horsthemke, B.6
-
15
-
-
0031085262
-
Estudio clínico, citogenético y molecular en 10 pacientes con síndrome de Prader-Willi
-
(Barc)
-
A. Barabash, M. Robledo, R. Sanz, M. Renedo, C. Ramos, C. Ayuso, et al. Estudio clínico, citogenético y molecular en 10 pacientes con síndrome de Prader-Willi Med Clin (Barc) 108 1997 304 306
-
(1997)
Med Clin
, vol.108
, pp. 304-306
-
-
Barabash, A.1
Robledo, M.2
Sanz, R.3
Renedo, M.4
Ramos, C.5
Ayuso, C.6
-
17
-
-
70350566869
-
-
[tesis doctoral]. Bellaterra: Universitat Autònoma de Barcelona; [consultado 12/2/2008]. Disponible en:
-
Poyatos D. Diagnóstico citogenético y molecular de los síndromes de Prader-Willi y Angelman [tesis doctoral]. Bellaterra: Universitat Autònoma de Barcelona; 2006 [consultado 12/2/2008]. Disponible en: URL: http://www.tdx.cat/TDX-0119106-200034.
-
(2006)
Diagnóstico Citogenético Y Molecular de Los Síndromes de Prader-Willi Y Angelman
-
-
Poyatos, D.1
-
18
-
-
0026595355
-
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13
-
B. Dittrich, W.P. Robinson, H. Knoblauch, K. Buiting, K. Schmidt, G. Gillessen-Kaesbach, et al. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13 Hum Genet 90 1992 313 315
-
(1992)
Hum Genet
, vol.90
, pp. 313-315
-
-
Dittrich, B.1
Robinson, W.P.2
Knoblauch, H.3
Buiting, K.4
Schmidt, K.5
Gillessen-Kaesbach, G.6
-
19
-
-
0030579593
-
PW71 methylation test for Prader-Willi and Angelman syndromes
-
B. Dittrich, K. Buiting, and B. Horsthemke PW71 methylation test for Prader-Willi and Angelman syndromes Am J Med Genet 61 1996 196 197
-
(1996)
Am J Med Genet
, vol.61
, pp. 196-197
-
-
Dittrich, B.1
Buiting, K.2
Horsthemke, B.3
-
20
-
-
0028133293
-
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
-
J.S. Sutcliffe, M. Nakao, S. Christian, K.H. Orstavik, N. Tommerup, D.H. Ledbetter, et al. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region Nat Genet 8 1994 52 58
-
(1994)
Nat Genet
, vol.8
, pp. 52-58
-
-
Sutcliffe, J.S.1
Nakao, M.2
Christian, S.3
Orstavik, K.H.4
Tommerup, N.5
Ledbetter, D.H.6
-
22
-
-
0030916936
-
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus
-
M. Zeschnigk, C. Lich, K. Buiting, W. Doerfler, and B. Horsthemke A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus Eur J Hum Genet 5 1997 94 98
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 94-98
-
-
Zeschnigk, M.1
Lich, C.2
Buiting, K.3
Doerfler, W.4
Horsthemke, B.5
-
23
-
-
33846251452
-
Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes
-
C. Camprubí, M.D. Coll, S. Villatoro, E. Gabau, A. Kamli, M.J. Martínez, et al. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes Eur J Med Genet 50 2007 11 20
-
(2007)
Eur J Med Genet
, vol.50
, pp. 11-20
-
-
Camprubí, C.1
Coll, M.D.2
Villatoro, S.3
Gabau, E.4
Kamli, A.5
Martínez, M.J.6
-
24
-
-
0030954459
-
A case with 47 XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotype
-
A. Rego, M.D. Coll, M. Regal, M. Guitart, T. Escudero, and R.V. García-Mayor A case with 47 XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotype Horm Res 48 1997 44 46
-
(1997)
Horm Res
, vol.48
, pp. 44-46
-
-
Rego, A.1
Coll, M.D.2
Regal, M.3
Guitart, M.4
Escudero, T.5
García-Mayor, R.V.6
-
25
-
-
0029867499
-
Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee
-
ASHG/ACMG
-
ASHG/ACMG Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee Am J Hum Genet 58 1996 1085 1088
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1085-1088
-
-
-
26
-
-
70350571957
-
-
Clinical Molecular Genetics Society (CMGS) and European Molecular Genetics Quality Network (EMQN)
-
Harvey J, Voelckel M, Malzac P, Moncla A, Ramsden S, Matthijs G. Draft best practice guidelines for molecular analysis of Prader Willi and Angelman syndromes. Clinical Molecular Genetics Society (CMGS) and European Molecular Genetics Quality Network (EMQN) 2002.
-
(2002)
Draft Best Practice Guidelines for Molecular Analysis of Prader Willi and Angelman Syndromes
-
-
Harvey, J.1
Voelckel, M.2
Malzac, P.3
Moncla, A.4
Ramsden, S.5
Matthijs, G.6
-
27
-
-
0029985822
-
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient
-
Y. Sun, R.D. Nicholls, M.G. Butler, S. Saitoh, B.E. Hainline, and C.G. Palmer Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient Hum Mol Genet 5 1996 517 524
-
(1996)
Hum Mol Genet
, vol.5
, pp. 517-524
-
-
Sun, Y.1
Nicholls, R.D.2
Butler, M.G.3
Saitoh, S.4
Hainline, B.E.5
Palmer, C.G.6
-
28
-
-
0029918828
-
Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint
-
A. Schulze, C. Hansen, N.E. Skakkebaek, K. Brondum-Nielsen, D.H. Ledbeter, and N. Tommerup Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint Nat Genet 12 1996 452 454
-
(1996)
Nat Genet
, vol.12
, pp. 452-454
-
-
Schulze, A.1
Hansen, C.2
Skakkebaek, N.E.3
Brondum-Nielsen, K.4
Ledbeter, D.H.5
Tommerup, N.6
-
29
-
-
0030761243
-
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome
-
J.M. Conroy, T.A. Grebe, L.A. Becker, K. Tsuchiya, R.D. Nicholls, K. Buiting, et al. Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome Am J Hum Genet 61 1997 388 394
-
(1997)
Am J Hum Genet
, vol.61
, pp. 388-394
-
-
Conroy, J.M.1
Grebe, T.A.2
Becker, L.A.3
Tsuchiya, K.4
Nicholls, R.D.5
Buiting, K.6
-
30
-
-
0033364338
-
Prader-Willi syndrome is caused by disruption of the SNRPN gene
-
C.D. Kuslich, J.A. Kobori, G. Mohapatra, C. Gregorio-King, and T.A. Donlon Prader-Willi syndrome is caused by disruption of the SNRPN gene Am J Hum Genet 64 1999 70 76
-
(1999)
Am J Hum Genet
, vol.64
, pp. 70-76
-
-
Kuslich, C.D.1
Kobori, J.A.2
Mohapatra, G.3
Gregorio-King, C.4
Donlon, T.A.5
-
31
-
-
24044464247
-
Methylation-specific MLPA (MS-MLPA): Simultaneous detection of CpG methylation and copy number changes of up to 40 sequences
-
A.O. Nygren, N. Ameziane, H.M. Duarte, R.N. Vijzelaar, Q. Waisfisz, C.J. Hess, et al. Methylation-specific MLPA (MS-MLPA): Simultaneous detection of CpG methylation and copy number changes of up to 40 sequences Nucleic Acids Res 33 2005 e128
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Nygren, A.O.1
Ameziane, N.2
Duarte, H.M.3
Vijzelaar, R.N.4
Waisfisz, Q.5
Hess, C.J.6
-
32
-
-
38149068398
-
Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities
-
D.C. Bittel, N. Kibiryeva, and M.G. Butler Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities Genet Test 11 2007 467 475
-
(2007)
Genet Test
, vol.11
, pp. 467-475
-
-
Bittel, D.C.1
Kibiryeva, N.2
Butler, M.G.3
-
33
-
-
44349191455
-
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
-
T. Sahoo, D. Del Gaudio, J.R. German, M. Shinawi, S.U. Peters, R.E. Person, et al. Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster Nat Genet 40 2008 719 721
-
(2008)
Nat Genet
, vol.40
, pp. 719-721
-
-
Sahoo, T.1
Del Gaudio, D.2
German, J.R.3
Shinawi, M.4
Peters, S.U.5
Person, R.E.6
-
34
-
-
0036918137
-
Relationship between clinical and genetic diagnosis of Prader-Willi syndrome
-
J. Whittington, A. Holland, T. Webb, J. Butler, D. Clarke, and H. Boer Relationship between clinical and genetic diagnosis of Prader-Willi syndrome J Med Genet 39 2002 926 932
-
(2002)
J Med Genet
, vol.39
, pp. 926-932
-
-
Whittington, J.1
Holland, A.2
Webb, T.3
Butler, J.4
Clarke, D.5
Boer, H.6
-
36
-
-
33750128290
-
Expression of 4 genes between chromosome 15 breakpoints i and ii and behavioral outcomes in Prader-Willi syndrome
-
D.C. Bittel, N. Kibiryeva, and M.G. Butler Expression of 4 genes between chromosome 15 breakpoints i and ii and behavioral outcomes in Prader-Willi syndrome Pediatrics 118 2006 e1276 e1283
-
(2006)
Pediatrics
, vol.118
-
-
Bittel, D.C.1
Kibiryeva, N.2
Butler, M.G.3
-
37
-
-
0028067984
-
Diverse mutations of the P gene among African-Americans with type ii (tyrosinase-positive) oculocutaneous albinism (OCA2)
-
S.T. Lee, R.D. Nicholls, R.E. Schnur, L.C. Guida, J. Lu-Kuo, N.B. Spinner, et al. Diverse mutations of the P gene among African-Americans with type ii (tyrosinase-positive) oculocutaneous albinism (OCA2) Hum Mol Genet 3 1994 2047 2051
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2047-2051
-
-
Lee, S.T.1
Nicholls, R.D.2
Schnur, R.E.3
Guida, L.C.4
Lu-Kuo, J.5
Spinner, N.B.6
-
38
-
-
0035825226
-
Possible dosage effect of maternally expressed genes on visual recognition memory in Prader-Willi syndrome
-
B. Joseph, M. Egli, J.S. Sutcliffe, and T. Thompson Possible dosage effect of maternally expressed genes on visual recognition memory in Prader-Willi syndrome Am J Med Genet 105 2001 71 75
-
(2001)
Am J Med Genet
, vol.105
, pp. 71-75
-
-
Joseph, B.1
Egli, M.2
Sutcliffe, J.S.3
Thompson, T.4
-
39
-
-
0034902186
-
Kinetic form discrimination in Prader-Willi syndrome
-
R. Fox, G.S. Yang, I.D. Feurer, M.G. Butler, and T. Thompson Kinetic form discrimination in Prader-Willi syndrome J Intellect Disabil Res 45 2001 317 325
-
(2001)
J Intellect Disabil Res
, vol.45
, pp. 317-325
-
-
Fox, R.1
Yang, G.S.2
Feurer, I.D.3
Butler, M.G.4
Thompson, T.5
-
40
-
-
0036822094
-
A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS
-
T. Webb, J. Whittington, D. Clarke, H. Boer, J. Butler, and A. Holland A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS Clin Genet 62 2002 273 281
-
(2002)
Clin Genet
, vol.62
, pp. 273-281
-
-
Webb, T.1
Whittington, J.2
Clarke, D.3
Boer, H.4
Butler, J.5
Holland, A.6
-
41
-
-
0029907547
-
Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: Sex specific differences
-
J. Mitchell, A. Schinzel, S. Langlois, G. Gillessen-Kaesbach, S. Schuffenhauer, R. Michaelis, et al. Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: Sex specific differences Am J Med Genet 65 1996 133 136
-
(1996)
Am J Med Genet
, vol.65
, pp. 133-136
-
-
Mitchell, J.1
Schinzel, A.2
Langlois, S.3
Gillessen-Kaesbach, G.4
Schuffenhauer, S.5
Michaelis, R.6
-
42
-
-
0031015938
-
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15
-
DOI 10.1002/(SICI)1096-8628(19970211)68:4<433::AID-AJMG12>3.0.CO;2- T
-
S.B. Cassidy, M. Forsythe, S. Heeger, R.D. Nicholls, N. Schork, and P. Benn Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15 Am J Med Genet 68 1997 433 440 (Pubitemid 27073712)
-
(1997)
American Journal of Medical Genetics
, vol.68
, Issue.4
, pp. 433-440
-
-
Cassidy, S.B.1
Forsythe, M.2
Heeger, S.3
Nicholls, R.D.4
Schork, N.5
Benn, P.6
Schwartz, S.7
-
43
-
-
0030924840
-
Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15
-
DOI 10.1002/(SICI)1096-8628(19970711)71:1<106::AID-AJMG19>3.0.CO;2- Q
-
M. Gunay-Aygun, S. Heeger, S. Schwartz, and S.B. Cassidy Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15 Am J Med Genet 71 1997 106 110 (Pubitemid 27276708)
-
(1997)
American Journal of Medical Genetics
, vol.71
, Issue.1
, pp. 106-110
-
-
Gunay-Aygun, M.1
Heeger, S.2
Schwartz, S.3
Cassidy, S.B.4
-
44
-
-
2542487643
-
Psychotic disorders in Prader-Willi syndrome
-
A. Vogels, M. De Hert, M.J. Descheemaeker, V. Govers, K. Devriendt, E. Legius, et al. Psychotic disorders in Prader-Willi syndrome Am J Med Genet 2004 238 243
-
(2004)
Am J Med Genet
, pp. 238-243
-
-
Vogels, A.1
De Hert, M.2
Descheemaeker, M.J.3
Govers, V.4
Devriendt, K.5
Legius, E.6
-
45
-
-
0037065539
-
Psychotic illness in people with Prader-Willi syndrome due to chromosome 15 maternal uniparental disomy
-
H. Boer, A. Holland, J. Whittington, J. Butler, T. Webb, and D. Clarke Psychotic illness in people with Prader-Willi syndrome due to chromosome 15 maternal uniparental disomy Lancet 359 2002 135 136
-
(2002)
Lancet
, vol.359
, pp. 135-136
-
-
Boer, H.1
Holland, A.2
Whittington, J.3
Butler, J.4
Webb, T.5
Clarke, D.6
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