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Clinical Genetics
|
July 3, 1998
Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patients
P 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 analysis
V 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 study
A Aweimer, I El-Battrawy, I Akin, et al.
Experimental Gerontology
|
January 1, 1996
SV40-mediated immortalization of human fibroblasts
H 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 consequences
T 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 genotyping
J 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 mosaicism
G 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 language
Z H Rosser, T Zerjal, M E Hurles, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 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 patients
P 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 analysis
V 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 study
A Aweimer, I El-Battrawy, I Akin, et al.
Experimental Gerontology
|
January 1, 1996
SV40-mediated immortalization of human fibroblasts
H 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 consequences
T 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 genotyping
J 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 mosaicism
G 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 language
Z H Rosser, T Zerjal, M E Hurles, et al.
Page
of 3