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American Journal of Medical Genetics
|
May 3, 1996
Clinical and ultrastructural findings in three patients with geleophysic dysplasia
B F Pontz, H Stöss, F Henschke, et al.
American Journal of Medical Genetics
|
May 3, 1996
The spectrum of free neuraminic acid storage disease in childhood: clinical, morphological and biochemical observations in three non-Finnish patients
A C Sewell, C F Poets, I Degen, et al.
Klinische Wochenschrift
|
October 1, 1974
A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesis
W N Meigel, P K Müller, B F Pontz, et al.
American Journal of Medical Genetics
|
May 3, 1996
Type II collagenopathies: are there additional family members?
P Freisinger, J Bonaventure, H Stoess, et al.
Experientia
|
December 15, 1985
SV40 transformed fibroblasts recognize the same 140 kD fibronectin chemotactic fragment as non-transformed cells
A Albini, G Allavena, H Richter, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
December 1, 1993
[Osteogenesis imperfecta in childhood and adolescence]
R E Brenner, B Schiller, B F Pontz, et al.
Journal of Inherited Metabolic Disease
|
August 7, 2001
Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry
S Stadler, K Gempel, I Bieger, et al.
The Journal of Investigative Dermatology
|
September 1, 1997
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skin
N Hammami-Hauasli, D U Kalinke, H Schumann, et al.
Bone Marrow Transplantation
|
August 6, 2003
T-cell-depleted peripheral blood stem cell transplantation for alpha-mannosidosis
M H Albert, F Schuster, C Peters, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
American Journal of Medical Genetics
|
May 3, 1996
Clinical and ultrastructural findings in three patients with geleophysic dysplasia
B F Pontz, H Stöss, F Henschke, et al.
American Journal of Medical Genetics
|
May 3, 1996
The spectrum of free neuraminic acid storage disease in childhood: clinical, morphological and biochemical observations in three non-Finnish patients
A C Sewell, C F Poets, I Degen, et al.
Klinische Wochenschrift
|
October 1, 1974
A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesis
W N Meigel, P K Müller, B F Pontz, et al.
American Journal of Medical Genetics
|
May 3, 1996
Type II collagenopathies: are there additional family members?
P Freisinger, J Bonaventure, H Stoess, et al.
Experientia
|
December 15, 1985
SV40 transformed fibroblasts recognize the same 140 kD fibronectin chemotactic fragment as non-transformed cells
A Albini, G Allavena, H Richter, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
December 1, 1993
[Osteogenesis imperfecta in childhood and adolescence]
R E Brenner, B Schiller, B F Pontz, et al.
Journal of Inherited Metabolic Disease
|
August 7, 2001
Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry
S Stadler, K Gempel, I Bieger, et al.
The Journal of Investigative Dermatology
|
September 1, 1997
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skin
N Hammami-Hauasli, D U Kalinke, H Schumann, et al.
Bone Marrow Transplantation
|
August 6, 2003
T-cell-depleted peripheral blood stem cell transplantation for alpha-mannosidosis
M H Albert, F Schuster, C Peters, et al.
Page
of 4