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Birth Defects Original Article Series
|
January 1, 1987
The value of examining spontaneously aborted human embryos and placentas
H J Bruyere, S Arya, J S Kozel, et al.
The Journal of Pediatrics
|
January 1, 1982
Errors of morphogenesis: concepts and terms. Recommendations of an international working group
J Spranger, K Benirschke, J G Hall, et al.
European Journal of Human Genetics : EJHG
|
January 17, 2003
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome
M I Kavamura, M G Pomponi, M Zollino, et al.
American Journal of Medical Genetics
|
April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome
H Chen, L Immken, R Lachman, et al.
Birth Defects Original Article Series
|
January 1, 1977
The pallister mosaic syndrome
P D Pallister, L F Meisner, B R Elejalde, et al.
American Journal of Medical Genetics
|
February 5, 1998
Smith-Lemli-Opitz syndrome in Japan
M Tsukahara, K Fujisawa, K Yamamoto, et al.
Journal of Applied Microbiology
|
February 19, 2002
Salmonella enterica serotype Enteritidis phage types 4, 7, 6, 8, 13a, 29 and 34: a comparative analysis of genomic fingerprints from geographically distant isolates
Ernesto Liebana, L Garcia-Migura, J Guard-Petter, et al.
International Clinical Psychopharmacology
|
June 28, 2000
Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder
A Broocks, B Bandelow, A George, et al.
Cardiovascular and Interventional Radiology
|
December 28, 2025
Effectiveness and Safety of Image-Guided Renal Biopsies: Insights from 5,235 Procedures in the German Society for Interventional Radiology and Minimally Invasive Therapy (DeGIR) Registry
R Ocker-Serger, M Opitz, L Klüner, et al.
Clinical Genetics
|
May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasia
J D Wegenke, D T Uehling, J B Wear, et al.
Page
of 52
Search research articles
Search
Showing results (471-480 of 520) with videos related to
Sort By:
Page
of 52
Birth Defects Original Article Series
|
January 1, 1987
The value of examining spontaneously aborted human embryos and placentas
H J Bruyere, S Arya, J S Kozel, et al.
The Journal of Pediatrics
|
January 1, 1982
Errors of morphogenesis: concepts and terms. Recommendations of an international working group
J Spranger, K Benirschke, J G Hall, et al.
European Journal of Human Genetics : EJHG
|
January 17, 2003
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome
M I Kavamura, M G Pomponi, M Zollino, et al.
American Journal of Medical Genetics
|
April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome
H Chen, L Immken, R Lachman, et al.
Birth Defects Original Article Series
|
January 1, 1977
The pallister mosaic syndrome
P D Pallister, L F Meisner, B R Elejalde, et al.
American Journal of Medical Genetics
|
February 5, 1998
Smith-Lemli-Opitz syndrome in Japan
M Tsukahara, K Fujisawa, K Yamamoto, et al.
Journal of Applied Microbiology
|
February 19, 2002
Salmonella enterica serotype Enteritidis phage types 4, 7, 6, 8, 13a, 29 and 34: a comparative analysis of genomic fingerprints from geographically distant isolates
Ernesto Liebana, L Garcia-Migura, J Guard-Petter, et al.
International Clinical Psychopharmacology
|
June 28, 2000
Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder
A Broocks, B Bandelow, A George, et al.
Cardiovascular and Interventional Radiology
|
December 28, 2025
Effectiveness and Safety of Image-Guided Renal Biopsies: Insights from 5,235 Procedures in the German Society for Interventional Radiology and Minimally Invasive Therapy (DeGIR) Registry
R Ocker-Serger, M Opitz, L Klüner, et al.
Clinical Genetics
|
May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasia
J D Wegenke, D T Uehling, J B Wear, et al.
Page
of 52