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Journal of Medical Genetics
|
July 1, 1989
Severe Silver-Russell syndrome
D Donnai, E Thompson, J Allanson, et al.
Journal of Medical Genetics
|
November 1, 1989
Abnormal chromosome complement resulting from a familial inversion of chromosome 2
S Richter, B Lockwood, D Lockwood, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2009
Array CGH ends diagnostic odyssey for infant with features of Williams and Alagille syndrome
C Honeywell, L Gardin, C Jimenez-Rivera, et al.
Human Genetics
|
October 1, 1989
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis
D H Lockwood, A Farrier, F Hecht, et al.
Journal of Medical Genetics
|
December 1, 1992
The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes
R Hughes-Benzie, J Allanson, A Hunter, et al.
Australian Veterinary Journal
|
October 1, 1996
Lymphocystis disease in snapper (Pagrus auratus) from Spencer Gulf, South Australia
P J Durham, M J Allanson, W G Hutchinson
Gene Therapy
|
January 1, 1994
Transfection of proto oncogene c-jun into a mouse neuroblastoma cell line potentiates differentiation
J Allanson, A B Bond, J Morton, et al.
Obstetrics and Gynecology
|
September 1, 1992
Ultrasonographic measurements of fetal ear
T Shimizu, L Salvador, J Allanson, et al.
Journal of Medical Genetics
|
January 1, 1989
Duplication 6p and deletion 9p
C Lytle, J Wade, A Farrier, et al.
The Journal of Pediatrics
|
February 1, 1991
Combined transient and peripheral defects in tetrahydrobiopterin synthesis
J Allanson, R McInnes, L Bradley, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
Journal of Medical Genetics
|
July 1, 1989
Severe Silver-Russell syndrome
D Donnai, E Thompson, J Allanson, et al.
Journal of Medical Genetics
|
November 1, 1989
Abnormal chromosome complement resulting from a familial inversion of chromosome 2
S Richter, B Lockwood, D Lockwood, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2009
Array CGH ends diagnostic odyssey for infant with features of Williams and Alagille syndrome
C Honeywell, L Gardin, C Jimenez-Rivera, et al.
Human Genetics
|
October 1, 1989
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis
D H Lockwood, A Farrier, F Hecht, et al.
Journal of Medical Genetics
|
December 1, 1992
The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes
R Hughes-Benzie, J Allanson, A Hunter, et al.
Australian Veterinary Journal
|
October 1, 1996
Lymphocystis disease in snapper (Pagrus auratus) from Spencer Gulf, South Australia
P J Durham, M J Allanson, W G Hutchinson
Gene Therapy
|
January 1, 1994
Transfection of proto oncogene c-jun into a mouse neuroblastoma cell line potentiates differentiation
J Allanson, A B Bond, J Morton, et al.
Obstetrics and Gynecology
|
September 1, 1992
Ultrasonographic measurements of fetal ear
T Shimizu, L Salvador, J Allanson, et al.
Journal of Medical Genetics
|
January 1, 1989
Duplication 6p and deletion 9p
C Lytle, J Wade, A Farrier, et al.
The Journal of Pediatrics
|
February 1, 1991
Combined transient and peripheral defects in tetrahydrobiopterin synthesis
J Allanson, R McInnes, L Bradley, et al.
Page
of 5