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Beckwith Wiedemann Syndrome Genetics

July 7, 2024

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Beckwith–Wiedemann syndrome | European Journal of Human Genetics
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Beckwith–Wiedemann syndrome caused by maternally inherited mutation of an OCT-bindi…
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Beckwith-Wiedemann Syndrome: Symptoms, Cause, Diagnosis
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A mysterious method of gene control sheds its secrets | Science | AAAS
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Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with a…
Figure 1. [Map of the BWS locus on 11p15.5]. - GeneReviews® - NCBI Bookshelf
Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syn…
Figure 2. [Causes of Beckwith-Wiedemann syndrome by genetic mechanism]. - GeneRevie…
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Cellular and molecular mechanisms in BWS Beckwith-Wiedemann syndrome Carolina Curto…
Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposi…
Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann sy…
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BWS Genetics, AFP, and Scans — My BWS Baby
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JCI - Beckwith-Wiedemann syndrome: imprinting in clusters revisited
Frontiers | Diagnosis and Management of Beckwith-Wiedemann Syndrome
Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygot…
PDF] Beckwith-Wiedemann syndrome: imprinting in clusters revisited. | Semantic Scho…
Beckwith-Wiedemann syndrome: Video & Anatomy | Osmosis
Beckwith-Wiedemann syndrome: MedlinePlus Genetics
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Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2014;19:52-57]
IJMS | Free Full-Text | Molecular and Clinical Opposite Findings in 11p15.5 Associa…
PDF) Beckwith-Wiedemann syndrome
BWS Genetics, AFP, and Scans — My BWS Baby
Beckwith–Wiedemann syndrome demonstrates a role for epigenetic control of normal de…
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IJMS | Free Full-Text | A Beckwith–Wiedemann-Associated CDKN1C Mutation Allows the …
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Frontiers | Diagnosis and Management of Beckwith-Wiedemann Syndrome
Japanese and North American/European patients with Beckwith–Wiedemann syndrome have…
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Transcription alterations of KCNQ1 associated with imprinted methylation defects in…
Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjec…
Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndr…
Beckwith-Wiedemann Syndrome via the CDKN1C Gene Test - PreventionGenetics
IJMS | Free Full-Text | Clinical and Molecular Diagnosis of Beckwith-Wiedemann Synd…
Beckwith – Wiedemann syndrome (Genetics)
Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting c…
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Table 10.1 from 10 Beckwith-wiedemann Syndrome | Semantic Scholar
Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwit…
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First report of a successful pregnancy by preimplantation genetic testing for Beckw…
Frontiers | Diagnosis and Management of Beckwith-Wiedemann Syndrome
Growth Regulation, Imprinted Genes, and Chromosome 11p15.5 | Pediatric Research
Beckwith–Wiedemann and IMAGe syndromes: two very different disea | TACG
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Beckwith – Wiedemann syndrome (Genetics)
Silver-Russell syndrome: genetic basis and molecular genetic testing | Orphanet Jou…
Figure 3 from Epigenetics and imprinting in human disease. | Semantic Scholar
IJMS | Free Full-Text | Clinical and Molecular Diagnosis of Beckwith-Wiedemann Synd…
Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 impr…
Beckwith–Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with …
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Beckwith–Wiedemann syndrome: multiple molecular mechanisms
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Beckwith-Wiedemann & Russell-Silver Testing
PDF) Expert consensus document: Clinical and molecular diagnosis, screening and man…
Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis an…
Beckwith-Wiedemann Syndrome (BWS) - DoveMed
Beckwith–Wiedemann syndrome - Choufani - 2010 - American Journal of Medical Genetic…
Development of disease-specific growth charts for Korean children with Beckwith–Wie…
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Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without m…
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