Results 151 to 160 of about 14,149 (242)

Renal MRI radiomics in Beckwith-Wiedemann syndrome: a novel imaging approach for genotype identification. [PDF]

Orphanet J Rare Dis
Bai M, Wu X, Wang J, Zhang M, Qiao Z, Zhang L, Liu J.   +6 more
europepmc   +1 more source

Genomic landscape of paediatric adrenocortical tumours [PDF]

, 2015
et al,, Mardis, Elaine R, Wilson, Richard K   +2 more
core   +2 more sources

[Beckwith-Wiedemann syndrome with ganglioneuroblastoma: a case report]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi
Tou JF, Feng CY, Xu B, Ye JJ.
europepmc   +1 more source

Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site. [PDF]

Clin Epigenetics
Masubuchi H, Urakawa T, Kosaki R, Nishimura R, Wada Y, Dateki S, Yagasaki H, Kagawa R, Nishimura Y, Soejima H, Ogata T, Fukami M, Kagami M.   +12 more
europepmc   +1 more source

Postprandial Hypoglycemia in a Patient With Clinical Beckwith-Wiedemann Syndrome. [PDF]

JCEM Case Rep
London B, Corker LC, Deng L, Mani B, Murray A, Krishnamurthy M.   +5 more
europepmc   +1 more source

Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature. [PDF]

Ital J Pediatr, 2023
Elefante P, Spedicati B, Faletra F, Pignata L, Cerrato F, Riccio A, Barbi E, Memo L, Travan L.   +8 more
europepmc   +1 more source

Two Infants with Beckwith-Wiedemann Syndrome

Balkan Journal of Medical Genetics, 2010
Ratbi I, Elalaoui S, Sefiani A
doaj   +1 more source

Preconception Care and Treatment with Assisted Reproductive Technologies [PDF]

, 2006
David A. Grainger, Linda M. Frazier, Courtney A. Rowland, EH Stephen, B Rostad, C Gnoth, FC Wright, JP Toner, C Witsenburg, MAM Hassan, MS Neal, M Zitzmann, P Fedorcsak, LM Frazier, A Strandell, D Adamson, MA Reynolds, EG Papanikolaou, S Kashyap, FM Helmerhorst, K Aittomaki, K Aittomaki, N Burello, P Arnaud, J Halliday, O Lidegaard, SART/ASRM (The practice committee of the Society for Assisted Reproductive Technology and the American Society for Reproductive Medicine), BS Houmard, GL Ryan, S Murray, WA Grobman   +30 more
core   +1 more source

Beckwith-Wiedemann Syndrome

, 2013
Stephan Mose, Stephan Mose, Brandon J. Fisher, Iris Rusu, Charlie Ma, Lu Wang, Larry C. Daugherty, Brandon J. Fisher, Stephan Mose, Tod W. Speer, Tod W. Speer, Anthony E. Dragun, Rene Rubin, Claudia Rübe, James H. Brashears, Stephan Mose, James H. Brashears, Christian Weiss, Claus Roedel, Christian Weiss, Claus Roedel, Edward J. Gracely, Rene Rubin, Lindsay G. Jensen, Brent S. Rose, Loren K. Mell, Arno J. Mundt, Iris Rusu, Anthony E. Dragun, Anthony E. Dragun, Albert S. DeNittis, Christin A. Knowlton, Michelle Kolton Mackay, Yan Yu, Laura Doyle, Cheng B. Saw, Yan Yu, Laura Doyle, Ning J. Yue, Rene Rubin, Nisha R. Patel, Michael L. Wong, Brian F. Hasson, Daniel Yeung, Jatinder Palta, Christin A. Knowlton, Michelle Kolton Mackay, James H. Brashears, Anthony E. Dragun, Anthony E. Dragun, David E. Wazer, Anthony E. Dragun, Anthony E. Dragun, Stephan Mose, Susan M. Varnum, Marianne B. Sowa, William F. Morgan   +56 more
  +4 more sources

Thirteen cases support the clinical significance of imprinting center 1 (IC1) microdeletions in Beckwith-Wiedemann syndrome. [PDF]

Clin Epigenetics
Ding Q, Stander Z, Elizalde BJ, Stelmach ES, Duncan JC, Vidal-Folch N, Hasadsri L, Rumilla KM, Shen W.   +8 more
europepmc   +1 more source