-
1
-
-
0034089489
-
Analysis of CDKNIC in Beckwith Wiedemann syndrome
-
Algar E, Brickell S, Deeble G, et al 2000. Analysis of CDKNIC in Beckwith Wiedemann syndrome. Hum Mutat 15(6): 497-508.
-
(2000)
Hum Mutat
, vol.15
, Issue.6
, pp. 497-508
-
-
Algar, E.1
Brickell, S.2
Deeble, G.3
-
2
-
-
0019513956
-
An epidemiologic study of congenital malformations of the anterior abdominal wall in more than half a million consecutive live births
-
Baird PA, MacDonald EC. 1981. An epidemiologic study of congenital malformations of the anterior abdominal wall in more than half a million consecutive live births. Am J Hum Genet 33(3): 470-478.
-
(1981)
Am J Hum Genet
, vol.33
, Issue.3
, pp. 470-478
-
-
Baird, P.A.1
MacDonald, E.C.2
-
3
-
-
0003287122
-
Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of the kidneys and pancreas, and Leydig-cell hyperplasia. Another syndrome?
-
Los Angeles, CA
-
Beckwith J. 1963. Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of the kidneys and pancreas, and Leydig-cell hyperplasia. Another syndrome? Annual Meeting of the Western Society for Pediatric Research, Los Angeles, CA.
-
(1963)
Annual Meeting of the Western Society for Pediatric Research
-
-
Beckwith, J.1
-
4
-
-
0000077851
-
Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly
-
Beckwith J. 1969. Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly. Birth Defects Orig Artic Ser 2: 188-196.
-
(1969)
Birth Defects Orig Artic Ser
, vol.2
, pp. 188-196
-
-
Beckwith, J.1
-
5
-
-
0019410039
-
Wiedemann-Beckwith syndrome: Autosomal-dominant inheritance in a family
-
Best LG, Hoekstra RE. 1981. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family. Am J Med Genet 9(4): 291-299.
-
(1981)
Am J Med Genet
, vol.9
, Issue.4
, pp. 291-299
-
-
Best, L.G.1
Hoekstra, R.E.2
-
6
-
-
0020957731
-
The pre and postnatal appearance of the kidneys in Beckwith-Wiedemann Syndrome
-
Carseldine DB, Crocker EF, Walker AG, et al. 1983. The pre and postnatal appearance of the kidneys in Beckwith-Wiedemann Syndrome. Australas Radiol 27(1): 30-32.
-
(1983)
Australas Radiol
, vol.27
, Issue.1
, pp. 30-32
-
-
Carseldine, D.B.1
Crocker, E.F.2
Walker, A.G.3
-
7
-
-
0033377772
-
Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome
-
Caspary T, Cleary MA, Perlman EJ, et al. 1999. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome. Genes Dev 13(23): 3115-3124.
-
(1999)
Genes Dev
, vol.13
, Issue.23
, pp. 3115-3124
-
-
Caspary, T.1
Cleary, M.A.2
Perlman, E.J.3
-
8
-
-
13544250689
-
Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients
-
Chang AS, Moley KH, Wangler M, et al. 2005. Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. Fertil Steril 83(2): 349-354.
-
(2005)
Fertil Steril
, vol.83
, Issue.2
, pp. 349-354
-
-
Chang, A.S.1
Moley, K.H.2
Wangler, M.3
-
9
-
-
0025301158
-
Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome
-
Chitayat D, Rothchild A, Ling E, et al. 1990. Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome. Am J Med Genet 36(4): 434-439.
-
(1990)
Am J Med Genet
, vol.36
, Issue.4
, pp. 434-439
-
-
Chitayat, D.1
Rothchild, A.2
Ling, E.3
-
10
-
-
0023848705
-
Prenatal ultrasound diagnosis of macroglossia in the Wiedemann-Beckwith syndrome
-
Cobellis G, Iannoto P, Stabile M, et al. 1988. Prenatal ultrasound diagnosis of macroglossia in the Wiedemann-Beckwith syndrome. Prenat Diagn 8(1): 79-81.
-
(1988)
Prenat Diagn
, vol.8
, Issue.1
, pp. 79-81
-
-
Cobellis, G.1
Iannoto, P.2
Stabile, M.3
-
11
-
-
0031940675
-
Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann Syndrome Registry
-
DeBaun MR, Tucker MA. 1998. Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry. J Pediatr 132(3 Pt 1): 398-400.
-
(1998)
J Pediatr
, vol.132
, Issue.3 PART 1
, pp. 398-400
-
-
DeBaun, M.R.1
Tucker, M.A.2
-
12
-
-
0036182963
-
Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects
-
DeBaun MR, Niemitz EL, McNeil DE, et al. 2002. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. Am J Hum Genet 70(3): 604-611.
-
(2002)
Am J Hum Genet
, vol.70
, Issue.3
, pp. 604-611
-
-
DeBaun, M.R.1
Niemitz, E.L.2
McNeil, D.E.3
-
13
-
-
0037222510
-
Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19
-
DeBaun MR, Niemitz EL, Feinberg AP. 2003. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet 72(1): 156-160.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.1
, pp. 156-160
-
-
DeBaun, M.R.1
Niemitz, E.L.2
Feinberg, A.P.3
-
14
-
-
0032511642
-
Seven cases of Wiedemann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11
-
Dutly F, Baumer A, Kayserili H, et al. 1998. Seven cases of Wiedemann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11. Am J Med Genet 79(5): 347-353.
-
(1998)
Am J Med Genet
, vol.79
, Issue.5
, pp. 347-353
-
-
Dutly, F.1
Baumer, A.2
Kayserili, H.3
-
15
-
-
0028470672
-
Beckwith-Wiedemann syndrome
-
Elliott M, Maher ER. 1994. Beckwith-Wiedemann syndrome. J Med Genet 31(7): 560-564.
-
(1994)
J Med Genet
, vol.31
, Issue.7
, pp. 560-564
-
-
Elliott, M.1
Maher, E.R.2
-
16
-
-
0028124711
-
Clinical features and natural history of Beckwith-Wiedemann syndrome: Presentation of 74 new cases
-
Elliott M, Bayly R, Cole T, et al. 1994. Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases. Clin Genet 46(2): 168-174.
-
(1994)
Clin Genet
, vol.46
, Issue.2
, pp. 168-174
-
-
Elliott, M.1
Bayly, R.2
Cole, T.3
-
18
-
-
0034234863
-
Serum alpha-fetoprotein levels in Beckwith-Wiedemann syndrome
-
Everman DB, Shuman C, Dzolganovski B, et al. 2000. Serum alpha-fetoprotein levels in Beckwith-Wiedemann syndrome. J Pediatr 137(1): 123-127.
-
(2000)
J Pediatr
, vol.137
, Issue.1
, pp. 123-127
-
-
Everman, D.B.1
Shuman, C.2
Dzolganovski, B.3
-
19
-
-
18744432675
-
Subtle familial unbalanced translocation t(8;11)(p23.2;p5.5) in two fetuses with Beckwith-Wiedemann features
-
Fert-Ferrer S, Guichet A, Tantau J, et al. 2000. Subtle familial unbalanced translocation t(8;11)(p23.2;p5.5) in two fetuses with Beckwith-Wiedemann features. Prenat Diagn 20(6): 511-515.
-
(2000)
Prenat Diagn
, vol.20
, Issue.6
, pp. 511-515
-
-
Fert-Ferrer, S.1
Guichet, A.2
Tantau, J.3
-
20
-
-
0015881090
-
Wiedemann-Beckwith syndrome
-
Forrester RM. 1973. Wiedemann-Beckwith syndrome. Lancet 2(7819): 47.
-
(1973)
Lancet
, vol.2
, Issue.7819
, pp. 47
-
-
Forrester, R.M.1
-
21
-
-
18444369997
-
Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy
-
Goldman M, Smith A, Shuman C, et al. 2002. Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy. J Am Soc Nephrol 13(8): 2077-2084.
-
(2002)
J Am Soc Nephrol
, vol.13
, Issue.8
, pp. 2077-2084
-
-
Goldman, M.1
Smith, A.2
Shuman, C.3
-
22
-
-
0022389382
-
Beckwith-Wiedemann syndrome: Prenatal ultrasound diagnosis using standard kidney to abdominal circumference ratio
-
Grundy H, Wallon S, Burlbaw J, et al. 1985. Beckwith-Wiedemann syndrome: prenatal ultrasound diagnosis using standard kidney to abdominal circumference ratio. Am J Perinatol 2(3): 236-239.
-
(1985)
Am J Perinatol
, vol.2
, Issue.3
, pp. 236-239
-
-
Grundy, H.1
Wallon, S.2
Burlbaw, J.3
-
23
-
-
0034755986
-
Prenatal sonographic diagnosis of Beckwith-Wiedemann syndrome in association with a single umbilical artery
-
Hamada H, Fujiki Y, Obata-Yasuoka M, et al. 2001. Prenatal sonographic diagnosis of Beckwith-Wiedemann syndrome in association with a single umbilical artery. J Clin Ultrasound 29(9): 535-538.
-
(2001)
J Clin Ultrasound
, vol.29
, Issue.9
, pp. 535-538
-
-
Hamada, H.1
Fujiki, Y.2
Obata-Yasuoka, M.3
-
24
-
-
0038517691
-
Hepatoblastoma associated with Beckwith-Wiedemann syndrome and hemihypertrophy
-
Hamada Y, Takada K, Fukunaga S, et al. 2003. Hepatoblastoma associated with Beckwith-Wiedemann syndrome and hemihypertrophy. Pediatr Surg Int 19(1-2): 112-114.
-
(2003)
Pediatr Surg Int
, vol.19
, Issue.1-2
, pp. 112-114
-
-
Hamada, Y.1
Takada, K.2
Fukunaga, S.3
-
25
-
-
0031033941
-
Prenatal diagnosis of Beckwith-Wiedemann syndrome
-
Harker CP, Winter T 3rd, Mack L. 1997. Prenatal diagnosis of Beckwith-Wiedemann syndrome. AJR Am J Roentgenol 168(2): 520-522.
-
(1997)
AJR Am J Roentgenol
, vol.168
, Issue.2
, pp. 520-522
-
-
Harker, C.P.1
Winter III, T.2
Mack, L.3
-
26
-
-
0028068946
-
Prenatal ultrasound diagnosis of Beckwith-Wiedemann syndrome
-
Hewitt B, Bankier A. 1994. Prenatal ultrasound diagnosis of Beckwith-Wiedemann syndrome. Aust N Z J Obstet Gynaecol 34(4): 488-490.
-
(1994)
Aust N Z J Obstet Gynaecol
, vol.34
, Issue.4
, pp. 488-490
-
-
Hewitt, B.1
Bankier, A.2
-
27
-
-
0018830651
-
Association of the Beckwith-Wiedemann and prune belly syndromes
-
Knight JA, Palmer WM, Gardner AY, et al. 1980. Association of the Beckwith-Wiedemann and prune belly syndromes. Clin Pediatr (Phila) 19(7): 485-488.
-
(1980)
Clin Pediatr (Phila)
, vol.19
, Issue.7
, pp. 485-488
-
-
Knight, J.A.1
Palmer, W.M.2
Gardner, A.Y.3
-
28
-
-
0022657297
-
Antenatal sonographic appearance of Beckwith-Wiedemann syndrome
-
Koontz WL, Shaw LA, Lavery JP. 1986. Antenatal sonographic appearance of Beckwith-Wiedemann syndrome. J Clin Ultrasound 14(1): 57-59.
-
(1986)
J Clin Ultrasound
, vol.14
, Issue.1
, pp. 57-59
-
-
Koontz, W.L.1
Shaw, L.A.2
Lavery, J.P.3
-
29
-
-
0015508247
-
The Wiedemann-Beckwith syndrome: Genetic considerations and a diagnostic sign
-
Kosseff AL, Hermann J, Opitz JM. 1972. The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign. Lancet 1(7755): 844.
-
(1972)
Lancet
, vol.1
, Issue.7755
, pp. 844
-
-
Kosseff, A.L.1
Hermann, J.2
Opitz, J.M.3
-
30
-
-
0033609117
-
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
-
Lee MP, DeBaun MR, Mitsuya K, et al. 1999. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc Natl Acad Sci USA 96(9): 5203-5208.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, Issue.9
, pp. 5203-5208
-
-
Lee, M.P.1
DeBaun, M.R.2
Mitsuya, K.3
-
31
-
-
0024469913
-
Prenatal diagnosis and perinatal management of the Beckwith-Wiedemann syndrome: A case and review
-
Lodeiro JG, Byers JW, 3rd, Chuipek S, et al. 1989. Prenatal diagnosis and perinatal management of the Beckwith-Wiedemann syndrome: a case and review. Am J Perinatol 6(4): 446-449.
-
(1989)
Am J Perinatol
, vol.6
, Issue.4
, pp. 446-449
-
-
Lodeiro, J.G.1
Byers III, J.W.2
Chuipek, S.3
-
32
-
-
0016389956
-
Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome
-
Lubinsky M, Herrmann J, Kosseff AL, et al. 1974. Letter: autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome. Lancet 1(7863): 932-933.
-
(1974)
Lancet
, vol.1
, Issue.7863
, pp. 932-933
-
-
Lubinsky, M.1
Herrmann, J.2
Kosseff, A.L.3
-
33
-
-
0024433872
-
In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case report
-
Meizner I, Carmi R, Katz M, et al. 1989. In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case report. Eur J Obstet Gynecol Reprod Biol 32(3): 259-264.
-
(1989)
Eur J Obstet Gynecol Reprod Biol
, vol.32
, Issue.3
, pp. 259-264
-
-
Meizner, I.1
Carmi, R.2
Katz, M.3
-
34
-
-
6344263978
-
Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome
-
Niemitz EL, DeBaun MR, Fallon J, et al. 2004. Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome. Am J Hum Genet 75(5): 844-849.
-
(2004)
Am J Hum Genet
, vol.75
, Issue.5
, pp. 844-849
-
-
Niemitz, E.L.1
DeBaun, M.R.2
Fallon, J.3
-
35
-
-
0022470737
-
The Wiedemann-Beckwith syndrome: Pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity
-
Niikawa N, Ishikiriyama S, Takahashi S, et al. 1986. The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity. Am J Med Genet 24(1): 41-55.
-
(1986)
Am J Med Genet
, vol.24
, Issue.1
, pp. 41-55
-
-
Niikawa, N.1
Ishikiriyama, S.2
Takahashi, S.3
-
36
-
-
0020962748
-
Familial Wiedeman-Beckwith syndrome: Prenatal echography diagnosis and histologic confirmation
-
Nivelon-Chevallier A, Mavel A, Michiels R, et al. 1983. Familial Wiedeman-Beckwith syndrome: prenatal echography diagnosis and histologic confirmation. J Genet Hum 31(Suppl. 5): 397-402.
-
(1983)
J Genet Hum
, vol.31
, Issue.SUPPL. 5
, pp. 397-402
-
-
Nivelon-Chevallier, A.1
Mavel, A.2
Michiels, R.3
-
37
-
-
0027993769
-
Beckwith-Wiedemann syndrome: Difficulties with prenatal diagnosis
-
Nowotny T, Bollmann R, Pfeifer L, et al. 1994. Beckwith-Wiedemann syndrome: difficulties with prenatal diagnosis. Fetal Diagn Ther 9(4): 256-260.
-
(1994)
Fetal Diagn Ther
, vol.9
, Issue.4
, pp. 256-260
-
-
Nowotny, T.1
Bollmann, R.2
Pfeifer, L.3
-
38
-
-
0022910322
-
Wiedemann-Beckwith syndrome: Presentation of clinical and cytogenetic data on 22 new cases and review of the literature
-
Pettenati MJ, Haines JL, Higgins RR, et al. 1986. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Hum Genet 74(2): 143-154.
-
(1986)
Hum Genet
, vol.74
, Issue.2
, pp. 143-154
-
-
Pettenati, M.J.1
Haines, J.L.2
Higgins, R.R.3
-
39
-
-
0031127744
-
Intrauterine growth and ultrasound findings in fetuses with Beckwith-Wiedemann syndrome
-
Ranzini AC, Day-Salvatore D, Turner T, et al. 1997. Intrauterine growth and ultrasound findings in fetuses with Beckwith-Wiedemann syndrome. Obstet Gynecol 89(4): 538-542.
-
(1997)
Obstet Gynecol
, vol.89
, Issue.4
, pp. 538-542
-
-
Ranzini, A.C.1
Day-Salvatore, D.2
Turner, T.3
-
40
-
-
0037154001
-
Wiedemann-Beckwith syndrome: Further prenatal characterization of the condition
-
Reish O, Lerer I, Amiel A, et al. 2002. Wiedemann-Beckwith syndrome: further prenatal characterization of the condition. Am J Med Genet 107(3): 209-213.
-
(2002)
Am J Med Genet
, vol.107
, Issue.3
, pp. 209-213
-
-
Reish, O.1
Lerer, I.2
Amiel, A.3
-
41
-
-
0020638763
-
Beckwith-Wiedemann syndrome: Role of ultrasound in its management
-
Shah KJ. 1983. Beckwith-Wiedemann syndrome: role of ultrasound in its management. Clin Radiol 34(3): 313-319.
-
(1983)
Clin Radiol
, vol.34
, Issue.3
, pp. 313-319
-
-
Shah, K.J.1
-
42
-
-
0025004760
-
Prenatal ultrasound diagnosis of Beckwith-Wiedemann syndrome
-
Shah YG, Metlay L. 1990. Prenatal ultrasound diagnosis of Beckwith-Wiedemann syndrome. J Clin Ultrasound 18(7): 597-600.
-
(1990)
J Clin Ultrasound
, vol.18
, Issue.7
, pp. 597-600
-
-
Shah, Y.G.1
Metlay, L.2
-
44
-
-
0030823992
-
Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome
-
Slavotinek A, Gaunt L, Donnai D. 1997. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome. J Med Genet 34(10): 819-826.
-
(1997)
J Med Genet
, vol.34
, Issue.10
, pp. 819-826
-
-
Slavotinek, A.1
Gaunt, L.2
Donnai, D.3
-
45
-
-
0018835921
-
Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential
-
Sotelo-Avila C, Gonzalez-Crussi F, Fowler JW. 1980. Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential. J Pediatr 96(1): 47-50.
-
(1980)
J Pediatr
, vol.96
, Issue.1
, pp. 47-50
-
-
Sotelo-Avila, C.1
Gonzalez-Crussi, F.2
Fowler, J.W.3
-
46
-
-
0018938941
-
Wilms' tumor in a patient with an incomplete form of Beckwith-Wiedemann syndrome
-
Sotelo-Avila C, Gonzalez-Crussi F, Starling KA. 1980. Wilms' tumor in a patient with an incomplete form of Beckwith-Wiedemann syndrome. Pediatrics 66(1): 121-123.
-
(1980)
Pediatrics
, vol.66
, Issue.1
, pp. 121-123
-
-
Sotelo-Avila, C.1
Gonzalez-Crussi, F.2
Starling, K.A.3
-
47
-
-
0025891267
-
Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome
-
Viljoen DL, Jaquire Z, Woods DL. 1991. Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome. Prenat Diagn 11(3): 167-175.
-
(1991)
Prenat Diagn
, vol.11
, Issue.3
, pp. 167-175
-
-
Viljoen, D.L.1
Jaquire, Z.2
Woods, D.L.3
-
48
-
-
0020511170
-
Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome
-
Waziri M, Patil SR, Hanson JW, et al. 1983. Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr 102(6): 873-876.
-
(1983)
J Pediatr
, vol.102
, Issue.6
, pp. 873-876
-
-
Waziri, M.1
Patil, S.R.2
Hanson, J.W.3
-
49
-
-
0018872701
-
In utero diagnosis of Beckwith-Wiedemann syndrome by ultrasound
-
Weinstein L, Anderson C. 1980. In utero diagnosis of Beckwith-Wiedemann syndrome by ultrasound. Radiology 134(2): 474.
-
(1980)
Radiology
, vol.134
, Issue.2
, pp. 474
-
-
Weinstein, L.1
Anderson, C.2
-
50
-
-
0028303271
-
Beckwith-Wiedemann syndrome: Antenatal diagnosis
-
Whisson CC, Whyte A, Ziesing P. 1994. Beckwith-Wiedemann syndrome: antenatal diagnosis. Australas Radiol 38(2): 130-131.
-
(1994)
Australas Radiol
, vol.38
, Issue.2
, pp. 130-131
-
-
Whisson, C.C.1
Whyte, A.2
Ziesing, P.3
-
51
-
-
0024805861
-
Prenatal diagnosis of Wiedemann-Beckwith syndrome
-
Wieacker P, Wilhelm C, Greiner P, et al. 1989. Prenatal diagnosis of Wiedemann-Beckwith syndrome. J Perinat Med 17(5): 351-355.
-
(1989)
J Perinat Med
, vol.17
, Issue.5
, pp. 351-355
-
-
Wieacker, P.1
Wilhelm, C.2
Greiner, P.3
-
52
-
-
76549164702
-
Familial malformation complex with umbilical hernia and macroglossia - A 'new syndrome'?
-
Wiedemann HR. 1964. Familial malformation complex with umbilical hernia and macroglossia - a 'new syndrome'? J Genet Hum 13: 223-232.
-
(1964)
J Genet Hum
, vol.13
, pp. 223-232
-
-
Wiedemann, H.R.1
-
53
-
-
0022447267
-
Prenatal diagnosis of the Beckwith-Wiedemann syndrome
-
Winter SC, Curry CJ, Smith JC, et al. 1986. Prenatal diagnosis of the Beckwith-Wiedemann syndrome. Am J Med Genet 24(1): 137-141.
-
(1986)
Am J Med Genet
, vol.24
, Issue.1
, pp. 137-141
-
-
Winter, S.C.1
Curry, C.J.2
Smith, J.C.3
-
54
-
-
0019783458
-
Beckwith-Wiedemann (exomphalos-macroglossia-gigantism-EMG) syndrome and malignant lymphoma
-
Wojciechowski AH, Pritchard J. 1981. Beckwith-Wiedemann (exomphalos-macroglossia-gigantism-EMG) syndrome and malignant lymphoma. Eur J Pediatr 137(3): 317-321.
-
(1981)
Eur J Pediatr
, vol.137
, Issue.3
, pp. 317-321
-
-
Wojciechowski, A.H.1
Pritchard, J.2
|