Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Sparago, Angela
Russo, Silvia
Cerrato, Flavia
Ferraiuolo, Serena
Castorina, Pierangela
Selicorni, Angelo
Schwienbacher, Christine
Negrini, Massimo
Ferrero, Giovanni Battista
Silengo, Margherita Cirillo
Anichini, Cecilia
Larizza, Lidia
and
Riccio, Andrea
2007.
Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour.
Human Molecular Genetics,
Vol. 16,
Issue. 3,
p.
254.
Duselis, Amanda R.
and
Vrana, Paul B.
2007.
Assessment and disease comparisons of hybrid developmental defects.
Human Molecular Genetics,
Vol. 16,
Issue. 7,
p.
808.
Smith, Adam C
Choufani, Sanaa
Ferreira, Jose C
and
Weksberg, Rosanna
2007.
Growth Regulation, Imprinted Genes, and Chromosome 11p15.5.
Pediatric Research,
Vol. 61,
Issue. 5 Part 2,
p.
43R.
Haas, O.A.
and
Bodamer, O.
2008.
Genetik in der Pädiatrie als Interaktion zwischen Klinik und Labor.
Monatsschrift Kinderheilkunde,
Vol. 156,
Issue. 4,
p.
323.
McBride, Sean M.
and
Haas-Kogan, Daphne A.
2008.
Nutrient-sensitive, antagonistically pleiotropic genes and their contribution to malignant behavior.
Medical Hypotheses,
Vol. 70,
Issue. 2,
p.
444.
Lebiedzińska, Aneta
2008.
Poradnictwo genetyczne w zespole Beckwitha-Wiedemanna. Część I. Diagnoza fenotypowa i genetyczna.
Pediatria Polska,
Vol. 83,
Issue. 5,
p.
529.
Lebiedzińska, Aneta
and
Midro, Alina T.
2008.
Poradnictwo genetyczne w zespole Beckwitha-Wiedemanna. Część II. Oszacowanie prawdopodobieństwa powtórzenia się BWS i prognoza genetyczna.
Pediatria Polska,
Vol. 83,
Issue. 5,
p.
535.
Brown, Keith W.
Power, Frances
Moore, Beth
Charles, Adrian K.
and
Malik, Karim T.A.
2008.
Frequency and Timing of Loss of Imprinting at 11p13 and 11p15 in Wilms' Tumor Development.
Molecular Cancer Research,
Vol. 6,
Issue. 7,
p.
1114.
Sotos, Juan F.
and
Argente, Jesús
2008.
Overgrowth Disorders Associated with Tall Stature.
Advances in Pediatrics,
Vol. 55,
Issue. 1,
p.
213.
Foresta, Carlo
Zuccarello, Daniela
Garolla, Andrea
and
Ferlin, Alberto
2008.
Role of Hormones, Genes, and Environment in Human Cryptorchidism.
Endocrine Reviews,
Vol. 29,
Issue. 5,
p.
560.
Eggermann, Thomas
Eggermann, Katja
and
Schönherr, Nadine
2008.
Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome.
Trends in Genetics,
Vol. 24,
Issue. 4,
p.
195.
Bacchetta, J.
Liutkus, A.
Dodat, H.
and
Cochat, P.
2008.
Dysplasie rénale multikystique : mise au point et information pour les parents lors du diagnostic anténatal.
Archives de Pédiatrie,
Vol. 15,
Issue. 6,
p.
1107.
Perkins, Jonathan A
2009.
Overview of macroglossia and its treatment.
Current Opinion in Otolaryngology & Head & Neck Surgery,
Vol. 17,
Issue. 6,
p.
460.
Kim, Alex C.
Barlaskar, Ferdous M.
Heaton, Joanne H.
Else, Tobias
Kelly, Victoria R.
Krill, Kenneth T.
Scheys, Joshua O.
Simon, Derek P.
Trovato, Alessia
Yang, Wei-Hsiung
and
Hammer, Gary D.
2009.
In Search of Adrenocortical Stem and Progenitor Cells.
Endocrine Reviews,
Vol. 30,
Issue. 3,
p.
241.
Glaser, Rivka L.
and
Morison, Ian M.
2009.
Bioinformatics for Systems Biology.
p.
485.
Berdasco, Maria
and
Esteller, Manel
2009.
Molecular Pathology.
p.
151.
Gebert, Claudia
Wrenzycki, Christine
Herrmann, Doris
Gröger, Daniela
Thiel, Janina
Reinhardt, Richard
Lehrach, Hans
Hajkova, Petra
Lucas-Hahn, Andrea
Carnwath, Joseph W.
and
Niemann, Heiner
2009.
DNA methylation in the IGF2 intragenic DMR is re-established in a sex-specific manner in bovine blastocysts after somatic cloning.
Genomics,
Vol. 94,
Issue. 1,
p.
63.
Heaton, Joanne H.
and
Hammer, Gary D.
2009.
Adrenocortical Carcinoma.
p.
285.
Weksberg, Rosanna
Shuman, Cheryl
and
Beckwith, J Bruce
2010.
Beckwith–Wiedemann syndrome.
European Journal of Human Genetics,
Vol. 18,
Issue. 1,
p.
8.
Szymański, Maciej
and
Barciszewski, Jan
2010.
RNA Technologies and Their Applications.
p.
393.