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American Journal of Medical Genetics
|
October 1, 1991
Concordance of auriculo-cardiovascular-skeletal malformations: a new malformation complex in an infant of a diabetic mother?
M Berkenstadt, R Shtrausberg, R M Goodman, et al.
The British Journal of Ophthalmology
|
October 1, 1979
Lipoid proteinosis (Urbach-Wiethe syndrome)
V Feiler-Ofry, A Lewy, L Regenbogen, et al.
Clinical Genetics
|
March 1, 1979
Acrocephalopolysyndactyly type IV: a new genetic syndrome in 3 sibs
R M Goodman, M Sternberg, Y Shem-Tov, et al.
American Journal of Medical Genetics
|
January 1, 1981
Symphalangism with multiple anomalies of the hands and feet: a new genetic trait
Y Learman, M B Katznelson, B Bonné-Tamir, et al.
American Journal of Medical Genetics
|
February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology
Z Borochowitz, L O Langer, H E Gruber, et al.
Journal of Craniofacial Genetics and Developmental Biology
|
January 1, 1989
Newly recognized ectrodactyly/deafness syndrome
A Raas-Rothschild, A Aviram, T Ben-Ami, et al.
Journal De Genetique Humaine
|
June 1, 1973
Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?
Y Frank, M Ziprkowski, A Romano, et al.
Gynecologic and Obstetric Investigation
|
January 1, 1989
Transcervical chorionic villi sampling: a comparison between the silver cannula and the Portex catheter
G Barkai, J Rabinovici, R Chaki, et al.
Birth Defects Original Article Series
|
January 1, 1975
Four new heritable disorders of connective tissue
R M Goodman, E Gazit, M B Katznelson, et al.
Gynecologic and Obstetric Investigation
|
January 1, 1987
Amniotic fluid alpha-fetoprotein levels and fetal chromosomal abnormalities
G Barkai, M B Katznelson, R Chaki, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics
|
October 1, 1991
Concordance of auriculo-cardiovascular-skeletal malformations: a new malformation complex in an infant of a diabetic mother?
M Berkenstadt, R Shtrausberg, R M Goodman, et al.
The British Journal of Ophthalmology
|
October 1, 1979
Lipoid proteinosis (Urbach-Wiethe syndrome)
V Feiler-Ofry, A Lewy, L Regenbogen, et al.
Clinical Genetics
|
March 1, 1979
Acrocephalopolysyndactyly type IV: a new genetic syndrome in 3 sibs
R M Goodman, M Sternberg, Y Shem-Tov, et al.
American Journal of Medical Genetics
|
January 1, 1981
Symphalangism with multiple anomalies of the hands and feet: a new genetic trait
Y Learman, M B Katznelson, B Bonné-Tamir, et al.
American Journal of Medical Genetics
|
February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology
Z Borochowitz, L O Langer, H E Gruber, et al.
Journal of Craniofacial Genetics and Developmental Biology
|
January 1, 1989
Newly recognized ectrodactyly/deafness syndrome
A Raas-Rothschild, A Aviram, T Ben-Ami, et al.
Journal De Genetique Humaine
|
June 1, 1973
Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?
Y Frank, M Ziprkowski, A Romano, et al.
Gynecologic and Obstetric Investigation
|
January 1, 1989
Transcervical chorionic villi sampling: a comparison between the silver cannula and the Portex catheter
G Barkai, J Rabinovici, R Chaki, et al.
Birth Defects Original Article Series
|
January 1, 1975
Four new heritable disorders of connective tissue
R M Goodman, E Gazit, M B Katznelson, et al.
Gynecologic and Obstetric Investigation
|
January 1, 1987
Amniotic fluid alpha-fetoprotein levels and fetal chromosomal abnormalities
G Barkai, M B Katznelson, R Chaki, et al.
Page
of 5