Beckwith-Wiedemann Syndrome
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[1] L. Mack,et al. Prenatal diagnosis of Beckwith-Wiedemann syndrome. , 1986, AJR. American journal of roentgenology.
[2] J. Graham,et al. Longitudinal observations on 15 children with Wiedemann-Beckwith syndrome. , 1995, American journal of medical genetics.
[3] M. Cohen. Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth. , 1994, American journal of medical genetics.
[4] A. Feinberg,et al. The genetics of BWS associated tumors , 1999 .
[5] J. Allanson,et al. Follow-up study of patients with Wiedemann-Beckwith syndrome with emphasis on the change in facial appearance over time. , 1994, American journal of medical genetics.
[6] L. Bolund,et al. Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5). , 1993, Journal of medical genetics.
[7] Benjamin Tycko,et al. Tumour-suppressor activity of H19 RNA , 1993, Nature.
[8] R. Weksberg,et al. Disruption of insulin–like growth factor 2 imprinting in Beckwith–Wiedemann syndrome , 1993, Nature genetics.
[9] R. Weksberg,et al. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. , 1993, Human molecular genetics.
[10] M. Eccles,et al. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour , 1993, Nature.
[11] S. Ewanowski,et al. Central tongue reduction for macroglossia. , 1993, Plastic and reconstructive surgery.
[12] C. Junien,et al. Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event , 1993, European journal of human genetics : EJHG.
[13] C. Clericuzio. Clinical phenotypes and Wilms tumor. , 1993, Medical and pediatric oncology.
[14] D. Viljoen,et al. Molecular Investigation of Familial Beckwith-Wiedemann Syndrome: A Model for Paternal Imprinting , 1993, European journal of human genetics : EJHG.
[15] E. Amparo,et al. Wilms' tumor in a patient with Beckwith-Wiedemann syndrome: onset detected with 3-month serial sonography. , 1993, AJR. American journal of roentgenology.
[16] J. Allanson,et al. The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes. , 1992, Journal of medical genetics.
[17] L. Gaunt,et al. Beckwith-Wiedemann syndrome. , 1992, Journal of medical genetics.
[18] C. Junien. Beckwith-Wiedemann syndrome, tumourigenesis and imprinting , 1992, Current Biology.
[19] M. Mannens,et al. Imprinting and Beckwith-Wiedemann syndrome , 1992, The Lancet.
[20] D. Yousefzadeh. Neonatal and pediatric sonography. , 1992, Current opinion in radiology.
[21] C Junien,et al. Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females. , 1992, Journal of medical genetics.
[22] J. Clayton-Smith,et al. Monozygotic twinning and Wiedemann-Beckwith syndrome. , 1992, American journal of medical genetics.
[23] E. Engel,et al. Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection. , 1991, American journal of medical genetics.
[24] J. Gyftodimou,et al. Twinning and mitotic crossing-over: some possibilities and their implications. , 1991, American journal of human genetics.
[25] D. Viljoen,et al. Prenatal diagnosis in autosomal dominant Beckwith‐Wiedemann syndrome , 1991, Prenatal diagnosis.
[26] A. Steele,et al. Congenital hepatoblastoma and Beckwith-Wiedemann syndrome: a case study including DNA ploidy profiles of tumor and adrenal cytomegaly. , 1991, Pediatric pathology.
[27] D. Chitayat,et al. Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome. , 1990, American journal of medical genetics.
[28] B. Falkner,et al. Beckwith-Wiedemann Syndrome , 1990, Clinical pediatrics.
[29] J. Hall,et al. Genomic imprinting: review and relevance to human diseases. , 1990, American journal of human genetics.
[30] M. Mott,et al. Genomic imprinting and the Beckwith-Wiedemann syndrome. , 1990, American journal of human genetics.
[31] A. Olney. Overgrowth syndromes. , 1990, Pediatric annals.
[32] J. White,et al. Macroglossia: a review. , 1990, The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society.
[33] N. Kiviat,et al. Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor. , 1990, Pediatric pathology.
[34] S. Feinstein,et al. Prenatal Diagnosis and Perinatal Management of the Beckwith-Wiedeman Syndrome: A Case and Review , 1989, American journal of perinatology.
[35] R. Carmi,et al. In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case report. , 1989, European journal of obstetrics, gynecology, and reproductive biology.
[36] W. Cavenee,et al. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. , 1989, American journal of human genetics.
[37] C. Partsch,et al. Growth, bone maturation and pubertal development in children with the EMG‐syndrome , 1989, Clinical genetics.
[38] M. Cohen,et al. A comprehensive and critical assessment of overgrowth and overgrowth syndromes. , 1989, Advances in human genetics.
[39] A. Feinberg,et al. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. , 1989, American journal of human genetics.
[40] J. M. Optiz,et al. Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins. , 1988, American journal of medical genetics.
[41] F. Lonardo,et al. Prenatal ultrasound diagnosis of macroglossia in the Wiedemann‐Beckwith syndrome , 1988, Prenatal diagnosis.
[42] R. Salman. Oral manifestations of Beckwith-Wiedemann syndrome. , 1988, Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry.
[43] C. Curry,et al. Prenatal diagnosis of the Beckwith-Wiedemann syndrome. , 1997, American journal of medical genetics.
[44] S. Brown. Wiedemann-Beckwith syndrome in one of monozygotic twins. , 1986, Archives of disease in childhood.
[45] N. Niikawa,et al. The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity. , 1986, American journal of medical genetics.
[46] S. Shaffer,et al. Beckwith-Wiedemann syndrome: prenatal ultrasound diagnosis using standard kidney to abdominal circumference ratio. , 1985, American journal of perinatology.
[47] C. Turleau,et al. Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy. , 1985, Annales de genetique.
[48] S. Pueschel,et al. Chromosome 11 and Beckwith-Wiedemann syndrome. , 1984, The Journal of pediatrics.
[49] S. Patil,et al. Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. , 1983, The Journal of pediatrics.
[50] B. Trudinger,et al. The pre and postnatal appearance of the kidneys in Beckwith-Wiedemann Syndrome. , 1983, Australasian radiology.
[51] M. Davidian,et al. The placenta in familial beckwith-wiedemann syndrome. , 1982, Birth defects original article series.
[52] C. Chantler,et al. Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling. , 1980, Journal of medical genetics.
[53] L. Weinstein,et al. In utero diagnosis of Beckwith--Wiedemann syndrome by ultrasound. , 1980, Radiology.
[54] F. Gonzalez-crussi,et al. Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential. , 1980, The Journal of pediatrics.
[55] M. Bene. [The Wiedemann-Beckwith syndrome]. , 1978, Revista de pediatrie, obstetrica si ginecologie. Pediatria.
[56] A. Rosenthal,et al. Cardiovascular abnormalities in the Beckwith-Wiedemann syndrome. , 1977, American journal of diseases of children.
[57] R. M. Forrester. Wiedemann-Beckwith syndrome. , 1973, Lancet.
[58] J. Opitz,et al. The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign. , 1972, Lancet.
[59] V. McKusick,et al. THE BECKWITH-WIEDEMANN SYNDROME: THE EXOMPHALOS-MACROGLOSSIA-GIGANTISM SYNDROME , 1970 .
[60] V. McKusick,et al. The Beckwith-Wiedmann syndrome. , 1970, Medicine.
[61] J. Beckwith. Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly , 1969 .
[62] H. Wiedemann. E.M.G. SYNDROME AND CARBOHYDRATE METABOLISM , 1968 .
[63] C. Hawes,et al. Cytomegaly of the adrenal gland. , 1955, A.M.A. American journal of diseases of children.