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Nature
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January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's disease
P Edery, S Lyonnet, L M Mulligan, et al.
Human Molecular Genetics
|
April 1, 1994
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families
R McMahon, L M Mulligan, C S Healey, et al.
International Journal of Dermatology
|
November 23, 2021
Contextualization of skin cancer incidence rates across Costa Rican provinces
Benjamin Gallo Marin, David X Zheng, Andres Amaya, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 1997
Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation
O Gimm, D J Marsh, S D Andrew, et al.
Oncogene
|
December 14, 2004
A model for GFR alpha 4 function and a potential modifying role in multiple endocrine neoplasia 2
Judith B Vanhorne, Scott D Andrew, Karen J Harrison, et al.
Clinical Psychological Science : a Journal of the Association for Psychological Science
|
December 15, 2023
Examining Blunted Initial Response to Reward and Recent Suicidal Ideation in Children and Adolescents Using Event-Related Potentials: Failure to Conceptually Replicate Across Two Independent Samples
Austin J Gallyer, Kreshnik Burani, Elizabeth M Mulligan, et al.
Clinical Endocrinology
|
July 1, 1995
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma
C Eng, L M Mulligan, D P Smith, et al.
Annals of Surgical Oncology
|
July 22, 2024
The Utility of Sentinel Lymph Node Biopsy in Elderly Patients with Melanoma
Hanna Kakish, Carmen A Jung, Susan J Doh, et al.
The Laryngoscope
|
July 12, 2023
A Medicare Physician Fee Schedule Analysis of Reimbursement Trends in Laryngology from 2000 to 2021
James R Xu, Robert R Lorenz, Kathleen M Mulligan, et al.
American Journal of Human Genetics
|
May 1, 1985
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3
L M Mulligan, M A Phillips, C J Forster-Gibson, et al.
Page
of 37
Search research articles
Search
Showing results (271-280 of 364) with videos related to
Sort By:
Page
of 37
Nature
|
January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's disease
P Edery, S Lyonnet, L M Mulligan, et al.
Human Molecular Genetics
|
April 1, 1994
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families
R McMahon, L M Mulligan, C S Healey, et al.
International Journal of Dermatology
|
November 23, 2021
Contextualization of skin cancer incidence rates across Costa Rican provinces
Benjamin Gallo Marin, David X Zheng, Andres Amaya, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 1997
Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation
O Gimm, D J Marsh, S D Andrew, et al.
Oncogene
|
December 14, 2004
A model for GFR alpha 4 function and a potential modifying role in multiple endocrine neoplasia 2
Judith B Vanhorne, Scott D Andrew, Karen J Harrison, et al.
Clinical Psychological Science : a Journal of the Association for Psychological Science
|
December 15, 2023
Examining Blunted Initial Response to Reward and Recent Suicidal Ideation in Children and Adolescents Using Event-Related Potentials: Failure to Conceptually Replicate Across Two Independent Samples
Austin J Gallyer, Kreshnik Burani, Elizabeth M Mulligan, et al.
Clinical Endocrinology
|
July 1, 1995
Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma
C Eng, L M Mulligan, D P Smith, et al.
Annals of Surgical Oncology
|
July 22, 2024
The Utility of Sentinel Lymph Node Biopsy in Elderly Patients with Melanoma
Hanna Kakish, Carmen A Jung, Susan J Doh, et al.
The Laryngoscope
|
July 12, 2023
A Medicare Physician Fee Schedule Analysis of Reimbursement Trends in Laryngology from 2000 to 2021
James R Xu, Robert R Lorenz, Kathleen M Mulligan, et al.
American Journal of Human Genetics
|
May 1, 1985
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3
L M Mulligan, M A Phillips, C J Forster-Gibson, et al.
Page
of 37