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Journal of Thrombosis and Haemostasis : JTH
|
April 16, 2015
Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small-platelet thrombocytopenia
C Levin, A Koren, E Pretorius, et al.
Prenatal Diagnosis
|
March 4, 2000
Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in northern Israel using polymorphic DNA markers
A Shalata, H Mandel, C Dorche, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 16, 2013
Learning disabilities in Darier's disease patients
R Dodiuk-Gad, M Lerner, Z Breznitz, et al.
Nature Genetics
|
September 7, 2001
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin
E Sprecher, R Bergman, G Richard, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 20, 2012
Bacteriological aspects of Darier's disease
R Dodiuk-Gad, E Cohen-Barak, M Ziv, et al.
Prenatal Diagnosis
|
September 25, 2009
Dependence of maternal serum [AFP]/[hCG] median ratios on age of gestation: comparison of trisomy 21 to euploid pregnancies
N Marcus-Braun, O Birk, E Manor, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
November 27, 1999
Syndrome dimensions of the child behavior checklist and the teacher report form: a critical empirical evaluation
C A Hartman, J Hox, J Auerbach, et al.
The British Journal of Dermatology
|
October 17, 2015
Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects
R P Dodiuk-Gad, E Cohen-Barak, M Khayat, et al.
The British Journal of Dermatology
|
June 9, 2016
Response to 'Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects': reply from the authors
R P Dodiuk-Gad, E Cohen-Barak, M Khayat, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 119) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 119 results.
Journal of Thrombosis and Haemostasis : JTH
|
April 16, 2015
Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small-platelet thrombocytopenia
C Levin, A Koren, E Pretorius, et al.
Prenatal Diagnosis
|
March 4, 2000
Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in northern Israel using polymorphic DNA markers
A Shalata, H Mandel, C Dorche, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
February 16, 2013
Learning disabilities in Darier's disease patients
R Dodiuk-Gad, M Lerner, Z Breznitz, et al.
Nature Genetics
|
September 7, 2001
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin
E Sprecher, R Bergman, G Richard, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 20, 2012
Bacteriological aspects of Darier's disease
R Dodiuk-Gad, E Cohen-Barak, M Ziv, et al.
Prenatal Diagnosis
|
September 25, 2009
Dependence of maternal serum [AFP]/[hCG] median ratios on age of gestation: comparison of trisomy 21 to euploid pregnancies
N Marcus-Braun, O Birk, E Manor, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
November 27, 1999
Syndrome dimensions of the child behavior checklist and the teacher report form: a critical empirical evaluation
C A Hartman, J Hox, J Auerbach, et al.
The British Journal of Dermatology
|
October 17, 2015
Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects
R P Dodiuk-Gad, E Cohen-Barak, M Khayat, et al.
The British Journal of Dermatology
|
June 9, 2016
Response to 'Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects': reply from the authors
R P Dodiuk-Gad, E Cohen-Barak, M Khayat, et al.
Page
of 12