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The Journal of Pediatrics
|
August 1, 1981
Pseudo-Menke syndrome
N D Dinno, U Yacoub, W Holmes, et al.
The New England Journal of Medicine
|
May 28, 1981
Post-mortem diagnosis of osteogenesis imperfecta congenita by exhumation and radiologic examination
N D Dinno, J F Kadlec, J D Stokes
Cutis
|
August 1, 1977
Macrodactyly and epidermal nevus
N D Dinno, L G Owen, B Weisskopf, et al.
Birth Defects Original Article Series
|
January 1, 1976
Bilateral microcornea, coloboma, short stature and other skeletal anomalies - a new hereditary syndrome
N D Dinno, T Lawwill, A E Leggett, et al.
Journal of Medical Genetics
|
October 1, 1982
Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardation
P E Podruch, F S Yen, N D Dinno, et al.
Birth Defects Original Article Series
|
January 1, 1982
Midtrimester diagnosis of osteogenesis imperfecta, type II
N D Dinno, U A Yacoub, J F Kadlec, et al.
American Journal of Diseases of Children (1960)
|
January 1, 1985
Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding
J H Hersh, K S Dale, P S Gerald, et al.
Developmental Medicine and Child Neurology
|
December 1, 1981
Behavioral correlates in the happy puppet syndrome: a characteristic profile?
J H Hersh, A S Bloom, A W Zimmerman, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1987
Three conditions in neonatal asphyxiating thoracic dysplasia (Jeune) and short rib-polydactyly syndrome spectrum: a clinicopathologic study
S S Yang, L O Langer, A Cacciarelli, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
The Journal of Pediatrics
|
August 1, 1981
Pseudo-Menke syndrome
N D Dinno, U Yacoub, W Holmes, et al.
The New England Journal of Medicine
|
May 28, 1981
Post-mortem diagnosis of osteogenesis imperfecta congenita by exhumation and radiologic examination
N D Dinno, J F Kadlec, J D Stokes
Cutis
|
August 1, 1977
Macrodactyly and epidermal nevus
N D Dinno, L G Owen, B Weisskopf, et al.
Birth Defects Original Article Series
|
January 1, 1976
Bilateral microcornea, coloboma, short stature and other skeletal anomalies - a new hereditary syndrome
N D Dinno, T Lawwill, A E Leggett, et al.
Journal of Medical Genetics
|
October 1, 1982
Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardation
P E Podruch, F S Yen, N D Dinno, et al.
Birth Defects Original Article Series
|
January 1, 1982
Midtrimester diagnosis of osteogenesis imperfecta, type II
N D Dinno, U A Yacoub, J F Kadlec, et al.
American Journal of Diseases of Children (1960)
|
January 1, 1985
Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding
J H Hersh, K S Dale, P S Gerald, et al.
Developmental Medicine and Child Neurology
|
December 1, 1981
Behavioral correlates in the happy puppet syndrome: a characteristic profile?
J H Hersh, A S Bloom, A W Zimmerman, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1987
Three conditions in neonatal asphyxiating thoracic dysplasia (Jeune) and short rib-polydactyly syndrome spectrum: a clinicopathologic study
S S Yang, L O Langer, A Cacciarelli, et al.
Page
of 2