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P C Patsalis

Showing results (21-30 of 29) with videos related to

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Clinical Genetics|July 3, 1998
Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patientsP C Patsalis, C Sismani, M I Hadjimarcou, et al.
European Journal of Medical Genetics|June 23, 2007
Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysisV Velissariou, C Sismani, S Christopoulou, et al.
Journal of Internal Medicine|November 12, 2020
Abnormal thyroid function is common in takotsubo syndrome and depends on two distinct mechanisms: results of a multicentre observational studyA Aweimer, I El-Battrawy, I Akin, et al.
Experimental Gerontology|January 1, 1996
SV40-mediated immortalization of human fibroblastsH L Ozer, S S Banga, T Dasgupta, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
ESMO Gastrointestinal Oncology|February 6, 2026
Anti-EGFR re-challenge with chemotherapy in RAS wild-type advanced colorectal cancer (A-REPEAT study): efficacy and correlations with tissue and plasma genotypingJ Sgouros, A Eliades, K Papadopoulou, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicismG Karadima, M Bugge, P Nicolaidis, et al.
American Journal of Human Genetics|November 15, 2000
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by languageZ H Rosser, T Zerjal, M E Hurles, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Clinical Genetics|July 3, 1998
Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patientsP C Patsalis, C Sismani, M I Hadjimarcou, et al.
European Journal of Medical Genetics|June 23, 2007
Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysisV Velissariou, C Sismani, S Christopoulou, et al.
Journal of Internal Medicine|November 12, 2020
Abnormal thyroid function is common in takotsubo syndrome and depends on two distinct mechanisms: results of a multicentre observational studyA Aweimer, I El-Battrawy, I Akin, et al.
Experimental Gerontology|January 1, 1996
SV40-mediated immortalization of human fibroblastsH L Ozer, S S Banga, T Dasgupta, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
ESMO Gastrointestinal Oncology|February 6, 2026
Anti-EGFR re-challenge with chemotherapy in RAS wild-type advanced colorectal cancer (A-REPEAT study): efficacy and correlations with tissue and plasma genotypingJ Sgouros, A Eliades, K Papadopoulou, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicismG Karadima, M Bugge, P Nicolaidis, et al.
American Journal of Human Genetics|November 15, 2000
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by languageZ H Rosser, T Zerjal, M E Hurles, et al.
Pageof 3