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Clinical genetics

Showing results (401-410 of 7,173) with videos related to

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Clinical Genetics|November 10, 2022
Novel CNNM4 variant and clinical features of Jalili syndromeKhanti Rattanapornsompong, Patcharaporn Gavila, Somkanya Tungsanga, et al.
Clinical Genetics|November 8, 2022
PIK3CA somatic mutations as potential biomarker for immunotherapy in elder or TP53 mutated gastric cancer patientsJun Yao, Qing You, Xin Zhang, et al.
Clinical Genetics|November 13, 2022
Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three familiesAurélie Becker, Charlotte Felici, Laëtitia Lambert, et al.
Clinical Genetics|March 1, 2005
Identification of germline BRCA1 and BRCA2 genetic alterations in Greek breast cancer moderate-risk and low-risk individuals--correlation with clinicopathological dataA Kataki, Ip Gomatos, N Pararas, et al.
Clinical Genetics|February 1, 1992
Hereditary motor and sensory neuropathy type I, associated with aplasia cutis congenita: possible X-linked inheritanceD Castle, H Isaacs, M Ramsay, et al.
Clinical Genetics|February 1, 1992
A new form of X-linked, high-frequency, sensorineural deafnessD Wellesley, J Goldblatt
Clinical Genetics|February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new caseM Lerone, A Pessagno, A Taccone, et al.
Clinical Genetics|February 28, 2004
Involvement of gene-diet/drug interaction in DNA methylation and its contribution to complex diseases: from cancer to schizophreniaS M Singh, B Murphy, R L O'Reilly
Clinical Genetics|February 28, 2004
Notch signaling in development and diseaseJ A Harper, J S Yuan, J B Tan, et al.
Clinical Genetics|April 7, 2005
Is osseous dysplasia a primary feature of neurofibromatosis 1 (NF1)?S Alwan, S J Tredwell, J M Friedman
Pageof 718

Showing results (401-410 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|November 10, 2022
Novel CNNM4 variant and clinical features of Jalili syndromeKhanti Rattanapornsompong, Patcharaporn Gavila, Somkanya Tungsanga, et al.
Clinical Genetics|November 8, 2022
PIK3CA somatic mutations as potential biomarker for immunotherapy in elder or TP53 mutated gastric cancer patientsJun Yao, Qing You, Xin Zhang, et al.
Clinical Genetics|November 13, 2022
Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three familiesAurélie Becker, Charlotte Felici, Laëtitia Lambert, et al.
Clinical Genetics|March 1, 2005
Identification of germline BRCA1 and BRCA2 genetic alterations in Greek breast cancer moderate-risk and low-risk individuals--correlation with clinicopathological dataA Kataki, Ip Gomatos, N Pararas, et al.
Clinical Genetics|February 1, 1992
Hereditary motor and sensory neuropathy type I, associated with aplasia cutis congenita: possible X-linked inheritanceD Castle, H Isaacs, M Ramsay, et al.
Clinical Genetics|February 1, 1992
A new form of X-linked, high-frequency, sensorineural deafnessD Wellesley, J Goldblatt
Clinical Genetics|February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new caseM Lerone, A Pessagno, A Taccone, et al.
Clinical Genetics|February 28, 2004
Involvement of gene-diet/drug interaction in DNA methylation and its contribution to complex diseases: from cancer to schizophreniaS M Singh, B Murphy, R L O'Reilly
Clinical Genetics|February 28, 2004
Notch signaling in development and diseaseJ A Harper, J S Yuan, J B Tan, et al.
Clinical Genetics|April 7, 2005
Is osseous dysplasia a primary feature of neurofibromatosis 1 (NF1)?S Alwan, S J Tredwell, J M Friedman
Pageof 718