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American Journal of Medical Genetics
|
March 1, 1993
Pleiotropy in Coffin-Lowry syndrome: sensorineural hearing deficit and premature tooth loss as early manifestations
J K Hartsfield, B D Hall, A W Grix, et al.
American Journal of Medical Genetics
|
January 1, 1978
Normal intelligence in two children with Carpenter syndrome
J L Frias, A H Felman, A L Rosenbloom, et al.
The Journal of Pediatrics
|
August 7, 2001
The subtle facial signs of prenatal exposure to alcohol: an anthropometric approach
E S Moore, R E Ward, P L Jamison, et al.
Nature
|
June 11, 1981
Only one of two closely related yeast suppressor tRNA genes contains an intervening sequence
M V Olson, G S Page, A Sentenac, et al.
Clinical Genetics
|
May 1, 1979
Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndrome
C J Curry, W D Loughman, U Francke, et al.
Birth Defects Original Article Series
|
January 1, 1974
Langer-Giedion syndrome
B D Hall, L O Langer, A Giedion, et al.
The Journal of Rheumatology
|
September 1, 1993
Presentation of multicentric Castleman's disease with sicca syndrome, cardiomyopathy, palmar and plantar rash
S F Kingsmore, O E Silva, B D Hall, et al.
The Journal of Pediatrics
|
January 1, 1974
A pattern of craniofacial and limb defects secondary to aberrant tissue bands
K L Jones, D W Smith, B D Hall, et al.
Human Molecular Genetics
|
June 1, 1994
Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindred
L D Piersall, H C Dietz, B D Hall, et al.
Metal Ions in Biological Systems
|
January 1, 1997
Bioaccumulation of mercury in the aquatic food chain in newly flooded areas
R A Bodaly, V L St Louis, M J Paterson, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 208) with videos related to
Sort By:
Page
of 21
American Journal of Medical Genetics
|
March 1, 1993
Pleiotropy in Coffin-Lowry syndrome: sensorineural hearing deficit and premature tooth loss as early manifestations
J K Hartsfield, B D Hall, A W Grix, et al.
American Journal of Medical Genetics
|
January 1, 1978
Normal intelligence in two children with Carpenter syndrome
J L Frias, A H Felman, A L Rosenbloom, et al.
The Journal of Pediatrics
|
August 7, 2001
The subtle facial signs of prenatal exposure to alcohol: an anthropometric approach
E S Moore, R E Ward, P L Jamison, et al.
Nature
|
June 11, 1981
Only one of two closely related yeast suppressor tRNA genes contains an intervening sequence
M V Olson, G S Page, A Sentenac, et al.
Clinical Genetics
|
May 1, 1979
Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndrome
C J Curry, W D Loughman, U Francke, et al.
Birth Defects Original Article Series
|
January 1, 1974
Langer-Giedion syndrome
B D Hall, L O Langer, A Giedion, et al.
The Journal of Rheumatology
|
September 1, 1993
Presentation of multicentric Castleman's disease with sicca syndrome, cardiomyopathy, palmar and plantar rash
S F Kingsmore, O E Silva, B D Hall, et al.
The Journal of Pediatrics
|
January 1, 1974
A pattern of craniofacial and limb defects secondary to aberrant tissue bands
K L Jones, D W Smith, B D Hall, et al.
Human Molecular Genetics
|
June 1, 1994
Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindred
L D Piersall, H C Dietz, B D Hall, et al.
Metal Ions in Biological Systems
|
January 1, 1997
Bioaccumulation of mercury in the aquatic food chain in newly flooded areas
R A Bodaly, V L St Louis, M J Paterson, et al.
Page
of 21