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Nature|January 15, 1998

A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.

Gynecologic Oncology|January 4, 2021

Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patientsHeather Hampel, Rachel Pearlman, Albert de la Chapelle, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.

Gut|August 5, 2010

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial diseaseM O Woods, H B Younghusband, P S Parfrey, et al.

Blood Advances|March 8, 2021

Gene expression signature predicts relapse in adult patients with cytogenetically normal acute myeloid leukemiaChristopher J Walker, Krzysztof Mrózek, Hatice Gulcin Ozer, et al.

Blood|May 17, 2003

BAALC expression predicts clinical outcome of de novo acute myeloid leukemia patients with normal cytogenetics: a Cancer and Leukemia Group B StudyClaudia D Baldus, Stephan M Tanner, Amy S Ruppert, et al.

Human Genetics|April 3, 2001

Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.

Medicine|October 6, 2020

A strobe multicenter descriptive study of 55 infectious aortitisLouis Journeau, Marine de la Chapelle, Thomas Guimard, et al.

Leukemia|November 16, 2016

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemiaA-K Eisfeld, J Kohlschmidt, S Schwind, et al.

Science (New York, N.Y.)|April 9, 2011

Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD IHuiling He, Sandya Liyanarachchi, Keiko Akagi, et al.

Pageof 61

Showing results (541-550 of 603) with videos related to

Sort By:

Pageof 61

Nature|January 15, 1998

A serine/threonine kinase gene defective in Peutz-Jeghers syndromeA Hemminki, D Markie, I Tomlinson, et al.

Gynecologic Oncology|January 4, 2021

Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patientsHeather Hampel, Rachel Pearlman, Albert de la Chapelle, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.

Gut|August 5, 2010

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial diseaseM O Woods, H B Younghusband, P S Parfrey, et al.

Blood Advances|March 8, 2021

Gene expression signature predicts relapse in adult patients with cytogenetically normal acute myeloid leukemiaChristopher J Walker, Krzysztof Mrózek, Hatice Gulcin Ozer, et al.

Blood|May 17, 2003

BAALC expression predicts clinical outcome of de novo acute myeloid leukemia patients with normal cytogenetics: a Cancer and Leukemia Group B StudyClaudia D Baldus, Stephan M Tanner, Amy S Ruppert, et al.

Human Genetics|April 3, 2001

Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.

Medicine|October 6, 2020

A strobe multicenter descriptive study of 55 infectious aortitisLouis Journeau, Marine de la Chapelle, Thomas Guimard, et al.

Leukemia|November 16, 2016

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemiaA-K Eisfeld, J Kohlschmidt, S Schwind, et al.

Science (New York, N.Y.)|April 9, 2011

Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD IHuiling He, Sandya Liyanarachchi, Keiko Akagi, et al.

Pageof 61