M. Susman

发表

Presenting signs of retinoblastoma.

D. Abramson, I. Dunkel, C. M. Frank, 1998, The Journal of pediatrics.

Quantitation of chromosome 1p and 19q deletions in glial tumours by interphase FISH on formalin-fixed paraffin-embedded tissue

S. Dale, J. Mills, M. Gonzales, 2006, Journal of Clinical Neuroscience.

Sarcomatoid renal cell carcinoma of papillary origin. A case report and cytogenic evaluation.

J. McNeal, R. Cohen, B. Iacopetta, 2000, Archives of pathology & laboratory medicine.

The Aicardi Syndrome in a 47, XXY Male

E. K. Turner, C. Keith, G. C. Webb, 1979, Australian paediatric journal.

Gonadoblastoma progressing to dysgerminoma in a 55-year-old woman with normal karyotype: follow-up studies.

C. Cooper, J. Carter, P. Russell, 2008, Pathology.

Posterior urethral valve: transperineal US for imaging and diagnosis in male infants.

H. Cohen, J. Haller, K. Glassberg, 1994, Radiology.

Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis

R. Gardner, S. Wilson, A. Daniel, 2002, Prenatal diagnosis.

Sarcomatoid Renal Cell Carcinoma of Papillary Origin

J. McNeal, R. Cohen, B. Iacopetta, 2000 .

Using population-based data to predict the impact of introducing noninvasive prenatal diagnosis for Down syndrome

E. Muggli, D. Amor, J. Halliday, 2010, Genetics in Medicine.

Dysembryoplastic neuroepithelial tumor (DNT)‐like oligodendrogliomas or DNTs evolving into oligodendrogliomas: Two illustrative cases

J. Laidlaw, W. Maixner, S. Dale, 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.

46,XX/46,XY at amniocentesis in a fetus with true hermaphroditism

M. Delatycki, J. Hutson, D. Amor, 1999, Journal of medical genetics.