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American Journal of Medical Genetics
|
January 1, 1985
X-linked dominant chondrodysplasia punctata: a case report and family studies
R F Mueller, P M Crowle, R A Jones, et al.
Hemoglobin
|
January 1, 1983
Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line
R F Mueller, J C Murray, R Gelinas, et al.
Biotechnology and Bioengineering
|
May 1, 1992
Characterization of initial events in bacterial surface colonization by two Pseudomonas species using image analysis
R F Mueller, W G Characklis, W L Jones, et al.
Journal of Medical Genetics
|
May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?
R M Winter, M A Patton, J Challener, et al.
Journal of Medical Genetics
|
September 1, 1989
Duplication of distal 17q from a maternal translocation: an additional case with some unique features
A Caine, D M Knapton, R F Mueller, et al.
British Journal of Obstetrics and Gynaecology
|
January 1, 1997
Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme
E Sheridan, J Williams, A Caine, et al.
The New England Journal of Medicine
|
September 8, 1983
Evaluation of a protocol for post-mortem examination of stillbirths
R F Mueller, V P Sybert, J Johnson, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation
T P Hutchin, N J Lench, S Arbuzova, et al.
Journal of Medical Genetics
|
November 1, 1988
The oculocerebrocutaneous (Delleman) syndrome
L I al-Gazali, D Donnai, S A Berry, et al.
Archives of Disease in Childhood
|
February 24, 2000
Proteus syndrome and immunodeficiency
D Hodge, S A Misbah, R F Mueller, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
January 1, 1985
X-linked dominant chondrodysplasia punctata: a case report and family studies
R F Mueller, P M Crowle, R A Jones, et al.
Hemoglobin
|
January 1, 1983
Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line
R F Mueller, J C Murray, R Gelinas, et al.
Biotechnology and Bioengineering
|
May 1, 1992
Characterization of initial events in bacterial surface colonization by two Pseudomonas species using image analysis
R F Mueller, W G Characklis, W L Jones, et al.
Journal of Medical Genetics
|
May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?
R M Winter, M A Patton, J Challener, et al.
Journal of Medical Genetics
|
September 1, 1989
Duplication of distal 17q from a maternal translocation: an additional case with some unique features
A Caine, D M Knapton, R F Mueller, et al.
British Journal of Obstetrics and Gynaecology
|
January 1, 1997
Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme
E Sheridan, J Williams, A Caine, et al.
The New England Journal of Medicine
|
September 8, 1983
Evaluation of a protocol for post-mortem examination of stillbirths
R F Mueller, V P Sybert, J Johnson, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation
T P Hutchin, N J Lench, S Arbuzova, et al.
Journal of Medical Genetics
|
November 1, 1988
The oculocerebrocutaneous (Delleman) syndrome
L I al-Gazali, D Donnai, S A Berry, et al.
Archives of Disease in Childhood
|
February 24, 2000
Proteus syndrome and immunodeficiency
D Hodge, S A Misbah, R F Mueller, et al.
Page
of 9