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1                                              Beckwith-Wiedemann spectrum (BWSp) is a prototypic CID r
2                                              Beckwith-Wiedemann syndrome (BWS) is a clinically variab
3                                              Beckwith-Wiedemann syndrome (BWS) is a congenital cancer
4                                              Beckwith-Wiedemann syndrome (BWS) is a fetal overgrowth
5                                              Beckwith-Wiedemann syndrome (BWS) is a hereditary human
6                                              Beckwith-Wiedemann syndrome (BWS) is a human stem cell d
7                                              Beckwith-Wiedemann syndrome (BWS) is a model human impri
8                                              Beckwith-Wiedemann syndrome (BWS) is an autosomal domina
9                                              Beckwith-Wiedemann syndrome (BWS), which causes prenatal
10                                              Beckwith-Wiedemann syndrome (BWS), which predisposes to
11 ing guidelines for neurofibromatosis type 1, Beckwith-Wiedemann syndrome/ hemihypertrophy, and PTEN h
12 abolic disorders such as type 2 diabetes and Beckwith-Wiedemann syndrome.
13 ted with the Prader-Willi Syndrome (PWS) and Beckwith-Wiedemann Syndrome (BWS) where imprinting is kn
14 line balanced chromosomal rearrangements and Beckwith-Wiedemann syndrome.
15 Prader-Willi syndrome, Angelman syndrome and Beckwith-Wiedemann syndrome.
16       This locus is of specific interest, as Beckwith-Wiedemann syndrome and various childhood and ad
17 associated with imprinting disorders such as Beckwith-Wiedemann syndrome (BWS).
18 s region to growth-related disorders such as Beckwith-Wiedemann syndrome and a variety of human cance
19 to develop rare epigenetic disorders such as Beckwith-Wiedemann Syndrome or Angelman Syndrome, both o
20 actor, along with genetic conditions such as Beckwith-Wiedemann syndrome, Simpson-Golabi-Behmel syndr
21  diseases associated with imprinting such as Beckwith-Wiedemann syndrome.
22  test on 18 patients potentially affected by Beckwith-Wiedemann syndrome, and 17 individuals with cel
23 them from the mutations of CDKN1C that cause Beckwith-Wiedemann syndrome, an overgrowth syndrome.
24 sing genes and loci, including those causing Beckwith-Wiedemann spectrum (BWSp) or WT1-related syndro
25 ergrowth and cancer predisposition condition Beckwith-Wiedemann syndrome (BWS).
26 1 that are associated with the human disease Beckwith-Wiedemann syndrome (BWS) may disrupt CDKN1C exp
27 nd genotypes characterize the human disease, Beckwith--Wiedemann syndrome (BWS).
28 s associated with the developmental disorder Beckwith Wiedemann Syndrome (BWS) and with several cance
29 ) we have found that the hereditary disorder Beckwith-Wiedemann syndrome, which predisposes to cancer
30  cause of the imprinting overgrowth disorder Beckwith-Wiedemann Syndrome (BWS).
31 mprinting-related fetal overgrowth disorder, Beckwith-Wiedemann syndrome.
32 gene is associated with the growth disorders Beckwith-Wiedemann and Silver-Russell syndromes and many
33 sociated with the human imprinting disorders Beckwith-Wiedemann syndrome (BWS) and Silver-Russell syn
34 on and the two contrasting growth disorders, Beckwith-Wiedemann syndrome (BWS) and Silver-Russell syn
35  employed, the cascade continues with a Dowd-Beckwith rearrangement and leads to the formation of the
36 l group migration, similar to that in a Dowd-Beckwith ring expansion.
37 enting classical approaches such as the Dowd-Beckwith reaction.
38          In these cases a fully equilibrated Beckwith-Houk-type transition state provides a satisfact
39 developing human brains and fibroblasts from Beckwith-Wiedemann syndrome patients.
40  lead to serious imprinting disorders (e.g., Beckwith-Wiedemann syndrome) and is described in some ca
41 mosome 11p15.1, centromeric to the imprinted Beckwith-Wiedemann syndrome (BWS) locus at 11p15.5.
42 of several pediatric and adult tumors and in Beckwith-Wiedemann syndrome (BWS).
43 ryonal tumors, including Wilms tumor, and in Beckwith-Wiedemann syndrome.
44  (ICR2), which is commonly hypomethylated in Beckwith-Wiedemann syndrome patients who exhibit massive
45 ome 11 at band p15.5, a region implicated in Beckwith-Wiedemann syndrome and a region of frequent los
46 s in human p57(Kip2) have been implicated in Beckwith-Wiedemann syndrome, a disease that has also bee
47 ed expression of IGF2 has been implicated in Beckwith-Wiedemann syndrome, a human fetal overgrowth sy
48 man chromosome 11p15.5, a region involved in Beckwith-Wiedemann syndrome, Wilms' tumor, and ovarian,
49 tes, a situation similar to that observed in Beckwith-Wiedemann syndrome, another imprinted disorder.
50 ncer and some hereditary diseases, including Beckwith-Wiedemann syndrome (BWS), a disorder of prenata
51          A related developmental disorder is Beckwith-Wiedemann syndrome (BWS), which increases risk
52                 A new class of chiral Karady-Beckwith dehydroalanines is designed and serves as a ver
53 ted with a human overgrowth syndrome-namely, Beckwith-Wiedemann syndrome (BWS).
54  Igf2 overexpression as a key determinant of Beckwith-Wiedemann syndrome.
55 all report an unexpectedly high incidence of Beckwith-Wiedemann syndrome (BWS) in children conceived
56 he mouse which will lead to animal models of Beckwith-Wiedemann syndrome and childhood tumours.
57 , are both implicated in the pathogenesis of Beckwith-Wiedemann syndrome.
58 , with six patients not showing phenotype of Beckwith-Wiedemann syndrome.
59 n of Igf2 results in most of the symptoms of Beckwith-Wiedemann syndrome, including prenatal overgrow
60 umor suppression and the cancer-predisposing Beckwith-Wiedemann syndrome (BWS).
61 implicated in the development of tumor-prone Beckwith-Wiedemann syndrome, is an effector molecule of
62 e patients with Prader-Willi syndrome (PWS), Beckwith-Wiedemann syndrome, Fragile-X syndrome, Angelma
63 imprinted status of the genes in the region, Beckwith-Wiedemann syndrome (BWS) and Wilms tumor are ea
64  during childhood, including retinoblastoma, Beckwith-Wiedemann syndrome/idiopathic hemihypertrophy a
65 roblasts derived from patients with sporadic Beckwith-Wiedemann syndrome (BWS), a fetal overgrowth sy
66 ype often associated with the human syndrome Beckwith-Wiedemann.
67 loss-of-imprinting (LOI) overgrowth syndrome Beckwith-Wiedemann (BWS).
68 re likely to develop the overgrowth syndrome Beckwith-Wiedemann (BWS).
69 und in the human foetal overgrowth syndrome, Beckwith-Wiedemann syndrome (BWS).
70                                          The Beckwith-Wiedemann syndrome (BWS) is genetically linked
71                                          The Beckwith-Wiedemann syndrome (BWS) is marked by fetal org
72                                          The Beckwith-Wiedemann syndrome is associated with the failu
73 ed groups, consistent with prediction by the Beckwith-Houk model for stereocontrol in 5-hexenyl radic
74 nkage analysis to harbor the gene(s) for the Beckwith-Wiedemann syndrome.
75 e p57(Kip2) locus has been implicated in the Beckwith-Wiedemann syndrome and in the development of sp
76 enal defects, which are also features of the Beckwith-Wiedemann syndrome (BWS), a genetically complex
77 ons affecting the WT1 gene or linkage to the Beckwith-Weidemann syndrome of the BWS region on the sho
78 ilms' tumors, and tumors associated with the Beckwith-Wiedemann syndrome.
79 H analysis to map the breakpoints from three Beckwith-Wiedemann syndrome patients and a rhabdoid tumo
80            Disruption of imprinting leads to Beckwith-Wiedemann syndrome (BWS), an overgrowth and can
81                 p57(Kip2) has been linked to Beckwith-Wiedemann syndrome and IMAGe syndrome in humans
82 educed H19 expression and is associated with Beckwith--Wiedemann syndrome (BWS).
83 , internal IC1 deletions are associated with Beckwith-Wiedemann syndrome (BWS) and Silver-Russell syn
84 imprinting region at 11p15.5 associated with Beckwith-Wiedemann syndrome.
85                                Children with Beckwith-Wiedemann syndrome (BWS) are at increased risk
86 uency of ART conceptions among children with Beckwith-Wiedemann syndrome or Angelman syndrome caused
87 ART was found in registries of children with Beckwith-Wiedemann syndrome, Angelman syndrome, and reti
88 variant that was identified in a family with Beckwith-Wiedemann syndrome and MLID.
89 n of human chromosome 11p15.5 is linked with Beckwith-Wiedemann syndrome that is associated with susc
90 from two infants with K(ATP)-HI and one with Beckwith-Weideman Syndrome-HI.
91 rearrangement breakpoints from patients with Beckwith-Wiedemann syndrome (BWS) have been mapped to 11
92 rearrangement breakpoints from patients with Beckwith-Wiedemann syndrome (BWS), a condition character
93  chromosomal rearrangements in patients with Beckwith-Wiedemann syndrome (BWS), which causes prenatal
94 he normal kidney and tongue of patients with Beckwith-Wiedemann syndrome (BWS), which predisposes to
95 their occasional occurrence in patients with Beckwith-Wiedemann syndrome and the case presented here
96 se phenotypes are also seen in patients with Beckwith-Wiedemann syndrome, a pleiotropic hereditary di