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Clinical Genetics
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August 1, 1987
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
H Eiberg, D Bixler, L S Nielsen, et al.
Clinical Genetics
|
March 1, 1979
The human X-chromosome and the levels of serum immunoglobulin M
V Escobar, L A Corey, D Bixler, et al.
American Journal of Human Genetics
|
November 1, 1986
Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data
C S Chung, D Bixler, T Watanabe, et al.
Oral Surgery, Oral Medicine, and Oral Pathology
|
October 1, 1977
Dentin dysplasia, type II: a rare autosomal dominant disorder
M Melnick, J R Eastman, L I Goldblatt, et al.
Pediatrics
|
August 1, 1990
Improved outcome in Pierre Robin sequence: effect of multidisciplinary evaluation and management
M J Bull, D C Givan, A M Sadove, et al.
Birth Defects Original Article Series
|
January 1, 1975
Diagnostic criteria for the whistling face syndrome
R M Antley, N Uga, N J Burzynski, et al.
American Journal of Diseases of Children (1960)
|
September 1, 1987
Urorectal septum malformation sequence. Report of six cases and embryological analysis
L F Escobar, D D Weaver, D Bixler, et al.
American Journal of Medical Genetics
|
August 1, 1990
Bone dysplasias: the prenatal diagnostic challenge
L F Escobar, D Bixler, D D Weaver, et al.
Journal of Craniofacial Genetics and Developmental Biology
|
January 1, 1990
A morphometric analysis of the fetal craniofacies by ultrasound: fetal cephalometry
L F Escobar, D Bixler, L M Padilla, et al.
Genetic Epidemiology
|
January 1, 1986
Human parotid proline-rich proteins: correlation of genetic polymorphisms to dental caries
P L Yu, D Bixler, P A Goodman, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 126) with videos related to
Sort By:
Page
of 13
Clinical Genetics
|
August 1, 1987
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
H Eiberg, D Bixler, L S Nielsen, et al.
Clinical Genetics
|
March 1, 1979
The human X-chromosome and the levels of serum immunoglobulin M
V Escobar, L A Corey, D Bixler, et al.
American Journal of Human Genetics
|
November 1, 1986
Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data
C S Chung, D Bixler, T Watanabe, et al.
Oral Surgery, Oral Medicine, and Oral Pathology
|
October 1, 1977
Dentin dysplasia, type II: a rare autosomal dominant disorder
M Melnick, J R Eastman, L I Goldblatt, et al.
Pediatrics
|
August 1, 1990
Improved outcome in Pierre Robin sequence: effect of multidisciplinary evaluation and management
M J Bull, D C Givan, A M Sadove, et al.
Birth Defects Original Article Series
|
January 1, 1975
Diagnostic criteria for the whistling face syndrome
R M Antley, N Uga, N J Burzynski, et al.
American Journal of Diseases of Children (1960)
|
September 1, 1987
Urorectal septum malformation sequence. Report of six cases and embryological analysis
L F Escobar, D D Weaver, D Bixler, et al.
American Journal of Medical Genetics
|
August 1, 1990
Bone dysplasias: the prenatal diagnostic challenge
L F Escobar, D Bixler, D D Weaver, et al.
Journal of Craniofacial Genetics and Developmental Biology
|
January 1, 1990
A morphometric analysis of the fetal craniofacies by ultrasound: fetal cephalometry
L F Escobar, D Bixler, L M Padilla, et al.
Genetic Epidemiology
|
January 1, 1986
Human parotid proline-rich proteins: correlation of genetic polymorphisms to dental caries
P L Yu, D Bixler, P A Goodman, et al.
Page
of 13