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G E Graham

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American Journal of Human Genetics|May 20, 1999

Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factorS Mardy, Y Miura, F Endo, et al.

Cancer Research|July 14, 1998

Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndromeJ M Carethers, F B Furnari, A F Zigman, et al.

Clinical Genetics|February 6, 2013

Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?M J M Nowaczyk, B A Thompson, S Zeesman, et al.

Clinical Oncology (Royal College of Radiologists (Great Britain))|August 6, 2019

Application of Hereditary Renal Cell Carcinoma Risk Criteria to a Large Prospective DatabaseI Kushnir, L Kirk, R Mallick, et al.

Clinical Genetics|August 19, 2015

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.

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Search research articles

Showing results (11-20 of 15) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 15 results.

American Journal of Human Genetics|May 20, 1999

Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factorS Mardy, Y Miura, F Endo, et al.

Cancer Research|July 14, 1998

Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndromeJ M Carethers, F B Furnari, A F Zigman, et al.

Clinical Genetics|February 6, 2013

Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?M J M Nowaczyk, B A Thompson, S Zeesman, et al.

Clinical Oncology (Royal College of Radiologists (Great Britain))|August 6, 2019

Application of Hereditary Renal Cell Carcinoma Risk Criteria to a Large Prospective DatabaseI Kushnir, L Kirk, R Mallick, et al.

Clinical Genetics|August 19, 2015

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.

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