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Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1975
Congenital trigeminal neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome)
S Aleksic, G Budzilovich, R Reuben, et al.
Journal of Neurosurgery
|
May 1, 1975
Radical one-stage correction of craniofacial anomalies
F J Epstein, D Wood-Smith, J M Converse, et al.
Developmental Medicine and Child Neurology
|
August 1, 1975
Unilateral arhinencephaly in goldenhar-gorlin syndrome
S Aleksic, G Budzilovich, R Reuben, et al.
Progress in Clinical and Biological Research
|
January 1, 1980
The current status of the major histocompatibility complex (HLA) in family studies of craniofacial developmental anomalies
F T Rapaport, J M Converse, J G McCarthy, et al.
Birth Defects Original Article Series
|
January 1, 1978
Recognition in adult patients of malformations induced by folic-acid antagonists
E W Reich, R P Cox, M H Becker, et al.
Transplantation Proceedings
|
December 1, 1973
Atypical patterns of inheritance of the serologically detectable (SD) products of the HL-A complex in human developmental anomalies
F T Rapaport, R Bachvaroff, J M Converse, et al.
Transplantation Proceedings
|
December 1, 1973
Genetic studies of mixed leukocyte culture reactivity in human developmental anomalies
F T Rapaport, R Bachvaroff, J M Converse, et al.
Bulletin of the Los Angeles Neurological Societies
|
April 1, 1976
Congenital facial neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome)
S Aleksic, G Budzilovich, R Reuben, et al.
Tissue Antigens
|
November 1, 1979
The major histocompatibility complex (HLA) as a genetic marker in human craniofacial anomalies
F T Rapaport, F H Bach, R J Bachvaroff, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1975
Congenital trigeminal neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome)
S Aleksic, G Budzilovich, R Reuben, et al.
Journal of Neurosurgery
|
May 1, 1975
Radical one-stage correction of craniofacial anomalies
F J Epstein, D Wood-Smith, J M Converse, et al.
Developmental Medicine and Child Neurology
|
August 1, 1975
Unilateral arhinencephaly in goldenhar-gorlin syndrome
S Aleksic, G Budzilovich, R Reuben, et al.
Progress in Clinical and Biological Research
|
January 1, 1980
The current status of the major histocompatibility complex (HLA) in family studies of craniofacial developmental anomalies
F T Rapaport, J M Converse, J G McCarthy, et al.
Birth Defects Original Article Series
|
January 1, 1978
Recognition in adult patients of malformations induced by folic-acid antagonists
E W Reich, R P Cox, M H Becker, et al.
Transplantation Proceedings
|
December 1, 1973
Atypical patterns of inheritance of the serologically detectable (SD) products of the HL-A complex in human developmental anomalies
F T Rapaport, R Bachvaroff, J M Converse, et al.
Transplantation Proceedings
|
December 1, 1973
Genetic studies of mixed leukocyte culture reactivity in human developmental anomalies
F T Rapaport, R Bachvaroff, J M Converse, et al.
Bulletin of the Los Angeles Neurological Societies
|
April 1, 1976
Congenital facial neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome)
S Aleksic, G Budzilovich, R Reuben, et al.
Tissue Antigens
|
November 1, 1979
The major histocompatibility complex (HLA) as a genetic marker in human craniofacial anomalies
F T Rapaport, F H Bach, R J Bachvaroff, et al.
Page
of 9