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searching for Beckwith–Wiedemann syndrome 11 found (82 total)

alternate case: beckwith–Wiedemann syndrome

RRM1 (988 words) [view diff] exact match in snippet view article find links to article

region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and

PHLDA2 (943 words) [view diff] exact match in snippet view article find links to article

region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and

Nephromegaly (115 words) [view diff] exact match in snippet view article find links to article

infancy and early childhood: A risk factor for Wilms tumor in Beckwith-Wiedemann syndrome". The Journal of Pediatrics. 132 (3). Elsevier BV: 401–404. doi:10

TSSC1 (471 words) [view diff] exact match in snippet view article find links to article

region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and

SLC22A18 (667 words) [view diff] exact match in snippet view article find links to article

region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and

Blastoma (1,699 words) [view diff] exact match in snippet view article find links to article

sometimes associated with specific genetic abnormalities such as the Beckwith-Wiedemann syndrome and familial adenomatous polyposis. The incidence has increased

NUP98 (1,515 words) [view diff] exact match in snippet view article find links to article

region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and

Combined bisulfite restriction analysis (1,300 words) [view diff] no match in snippet view article find links to article

methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann_syndrome, and characterizing DNA methylation patterns in the genome during

Developmental bioelectricity (17,264 words) [view diff] exact match in snippet view article find links to article

J.; Caluseriu, O.; et al. (2001). "Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15

Neural tube defect (5,814 words) [view diff] exact match in snippet view article find links to article

Hoving, Eelco (2008). ""Nasal encephalocele in a child with Beckwith-Wiedemann syndrome"". Journal of Neurosurgery. 6 (1): 485–7. doi:10.3171/PED/2008/1/6/485

Intragenomic and intrauterine conflict in humans (2,324 words) [view diff] case mismatch in snippet view article find links to article

inheritance patterns including Prader-Willi/Angelman Syndromes, Beckwith-Wiedemann Syndrome, and Silver-Russell Syndrome. Disorders of imprinting are thought