Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30‐year‐old mystery von Schimke, R. Neil, Collins, Debra L., Stolle, Catherine A.

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Preoperative Screening of Colorectal Cancers Is As Accurate As Postoperative Screening for Detection of Lynch Syndrome von Harrigan, Jack, Davis, Christian, Chauhan, Mahak, Buckles, Daniel, Saeed, Anwaar, Kennedy, Kevin, Collins, Debra L., Olyaee, Mojtaba, Madan, Rashna, Bansal, Ajay

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Schimke XLID syndrome results from a deletion in BCAP31 von Louie, Raymond J., Collins, Debra L., Friez, Michael J., Skinner, Cindy, Schwartz, Charles E., Stevenson, Roger E.

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Hereditary cancer screening: Case reports and review of literature on ten Ashkenazi Jewish founder mutations von Cox, Devin M., Nelson, Katherine L., Clytone, Meera, Collins, Debra L.

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Regarding cancer predisposition detected by CHG arrays von Collins, Debra L, Schimke, R Neil

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SchimkeXLIDsyndrome results from a deletion inBCAP31 von Louie, Raymond J., Collins, Debra L., Friez, Michael J., Skinner, Cindy, Schwartz, Charles E., Stevenson, Roger E.

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The Hunter–MacDonald syndrome with expanded phenotype including risk of meningioma: An update and review von Armstrong, Linlea, Graham, Gail E., Schimke, R. Neil, Collins, Debra L., Kirse, Daniel J., Costello, Fiona, Ardinger, Holly H.

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Regarding cancer predisposition detected by CHG arrays von Collins, Debra L, Schimke, R Neil

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Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene von Bradley, John F., Collins, Debra L., Schimke, R. Neil, Parrott, Heather N., Rothberg, Paul G.

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Schimke XLID syndrome results from a deletion in BCAP31 von Louie, Raymond J, Collins, Debra L, Friez, Michael J, Skinner, Cindy, Schwartz, Charles E, Stevenson, Roger E

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Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30-year-old mystery von Schimke, R. Neil, Collins, Debra L., Stolle, Catherine A.

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Response to Serville et al von Horton, William A., Harris, David J., Collins, Debra L.

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Innovations in human genetics education: College course work in human genetics for elementary, middle, and high school educators in Kansas von Collins, D L, Schimke, R N

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Diagnosis and management of asymptomatic renal cell carcinomas in von Hippel-Lindau syndrome von Levine, Errol, Weigel, John W., Collins, Debra L.

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The Hunter-MacDonald syndrome with expanded phenotype including risk of meningioma: An update and review von Armstrong, Linlea, Graham, Gail E., Schimke, R. Neil, Collins, Debra L., Kirse, Daniel J., Costello, Fiona, Ardinger, Holly H.

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Functioning carotid paraganglioma in the von Hippel-Lindau syndrome von Schimke, R. Neil, Collins, Debra L., Rothberg, Paul G.

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Congenital nonprogressive myopathy with Möbius and Robin sequence-the Carey-Fineman-Ziter syndrome: A confirmatory report von Schimke, R. Neil, Collins, Debra L., Hiebert, John M.

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Response to Serville et al von Horton, William A., Harris, David J., Collins, Debra L.

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Brachyolmia, recessive type (Hobaek): A clinical, radiographic, and histochemical study von Horton, William A., Langer, Leonard O., Collins, Debra L., Dwyer, Carmen

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A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness von Schimke, R. Neil, Horton, William A., Collins, Debra L., Therou, Leona, Opitz, John M.

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