Surgical Outcomes of Patients with Beckwith-Wiedemann Syndrome.
暂无分享,去创建一个
[1] J. Kalish,et al. Management of adrenal masses in patients with Beckwith–Wiedemann syndrome , 2017, Pediatric blood & cancer.
[2] Saskia M. J. Hopman,et al. Phenotype, cancer risk, and surveillance in Beckwith–Wiedemann syndrome depending on molecular genetic subgroups , 2016, American journal of medical genetics. Part A.
[3] S. Abramowicz,et al. Prevalence of Sleep-Disordered Breathing in Patients with Beckwith-Wiedemann Syndrome , 2014, The Journal of craniofacial surgery.
[4] J. Feusner,et al. Hepatoblastoma in Children With Beckwith-Wiedemann Syndrome: Does it Warrant Different Treatment? , 2014, Journal of pediatric hematology/oncology.
[5] R. Weksberg,et al. High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome , 2013, Human Genetics.
[6] J. McCarthy,et al. Guided growth for the treatment of limb length discrepancy: a comparative study of the three most commonly used surgical techniques , 2013, Journal of pediatric orthopedics. Part B.
[7] R. Weksberg,et al. Molecular Findings in Beckwith–Wiedemann Syndrome , 2013, American journal of medical genetics. Part C, Seminars in medical genetics.
[8] M. Abeleira,et al. A multidisciplinary approach to the treatment of oral manifestations associated with Beckwith-Wiedemann syndrome: a long-term case report. , 2011, Journal of the American Dental Association.
[9] K. V. van Lierde,et al. Impact of Tongue Reduction on Overall Speech Intelligibility, Articulation and Oromyofunctional Behavior in 4 Children with Beckwith-Wiedemann Syndrome , 2011, Folia Phoniatrica et Logopaedica.
[10] G. Mortier,et al. Long-term impact of tongue reduction on speech intelligibility, articulation and oromyofunctional behaviour in a child with Beckwith-Wiedemann syndrome. , 2010, International journal of pediatric otorhinolaryngology.
[11] L. Wilkins-Haug,et al. Outcome of fetuses with a prenatal ultrasound diagnosis of isolated omphalocele , 2009, Prenatal diagnosis.
[12] L. Wilkins-Haug,et al. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies. , 2009, Birth defects research. Part A, Clinical and molecular teratology.
[13] J. Haines,et al. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature , 1986, Human Genetics.
[14] Andrew P Feinberg,et al. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. , 2002, American journal of human genetics.
[15] D. Viljoen,et al. Prenatal diagnosis in autosomal dominant Beckwith‐Wiedemann syndrome , 1991, Prenatal diagnosis.
[16] J. Pensler,et al. The Efficacy of Tongue Resection in Treatment of Symptomatic Macroglossia in the Child , 1990, Annals of plastic surgery.
[17] Wiedemann Hr. [FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?] , 1964 .