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The Journal of Pediatrics
|
November 1, 1988
Postoperative dystonia in a female patient with homocystinuria
L Arbour, B Rosenblatt, C Clow, et al.
Annales De Genetique
|
January 5, 2002
Duplication 8 [inv dup(8)(p12p23)] with macrocephaly
V S Tonk, G N Wilson, G V Velagaleti
Journal of Medical Genetics
|
February 1, 1984
Cat eye syndrome owing to tetrasomy 22pter leads to q11
G N Wilson, D L Baker, J Schau, et al.
American Journal of Medical Genetics
|
July 1, 1993
Genomic imprinting: summary of an NICHD conference
G N Wilson, J G Hall, F de la Cruz
American Journal of Medical Genetics. Supplement
|
January 1, 1987
Effect of aneuploidy and neoplasia on human ribosomal DNA inheritance
G N Wilson, A Mian, J P de Chadarévian, et al.
Journal of Medical Genetics
|
June 1, 1985
Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes
G N Wilson, S E Sauder, M Bush, et al.
Molecular Biology and Evolution
|
April 1, 1984
Individual and evolutionary variation of primate ribosomal DNA transcription initiation regions
G N Wilson, M Knoller, L L Szura, et al.
The New England Journal of Medicine
|
July 25, 1985
Evidence that the human Y chromosome does not contain clustered DNA sequences (BKM) associated with heterogametic sex determination in other vertebrates
K Kiel-Metzger, G Warren, G N Wilson, et al.
Clinical Pediatrics
|
September 1, 1991
Gastrointestinal malformation in genetic disorders: a case of partial trisomy 2q with short esophagus and tubular stomach
J Porter, V R Klein, G N Wilson, et al.
Journal of Medical Genetics
|
September 1, 1992
Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11
G N Wilson, C S Richards, K Katz, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 88) with videos related to
Sort By:
Page
of 9
The Journal of Pediatrics
|
November 1, 1988
Postoperative dystonia in a female patient with homocystinuria
L Arbour, B Rosenblatt, C Clow, et al.
Annales De Genetique
|
January 5, 2002
Duplication 8 [inv dup(8)(p12p23)] with macrocephaly
V S Tonk, G N Wilson, G V Velagaleti
Journal of Medical Genetics
|
February 1, 1984
Cat eye syndrome owing to tetrasomy 22pter leads to q11
G N Wilson, D L Baker, J Schau, et al.
American Journal of Medical Genetics
|
July 1, 1993
Genomic imprinting: summary of an NICHD conference
G N Wilson, J G Hall, F de la Cruz
American Journal of Medical Genetics. Supplement
|
January 1, 1987
Effect of aneuploidy and neoplasia on human ribosomal DNA inheritance
G N Wilson, A Mian, J P de Chadarévian, et al.
Journal of Medical Genetics
|
June 1, 1985
Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes
G N Wilson, S E Sauder, M Bush, et al.
Molecular Biology and Evolution
|
April 1, 1984
Individual and evolutionary variation of primate ribosomal DNA transcription initiation regions
G N Wilson, M Knoller, L L Szura, et al.
The New England Journal of Medicine
|
July 25, 1985
Evidence that the human Y chromosome does not contain clustered DNA sequences (BKM) associated with heterogametic sex determination in other vertebrates
K Kiel-Metzger, G Warren, G N Wilson, et al.
Clinical Pediatrics
|
September 1, 1991
Gastrointestinal malformation in genetic disorders: a case of partial trisomy 2q with short esophagus and tubular stomach
J Porter, V R Klein, G N Wilson, et al.
Journal of Medical Genetics
|
September 1, 1992
Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11
G N Wilson, C S Richards, K Katz, et al.
Page
of 9