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Pediatrics
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March 1, 1979
Strychnine therapy in nonketotic hyperglycinemia
D Arneson, L T Ch'ien, P Chance, et al.
Birth Defects Original Article Series
|
January 1, 1977
Familial fatal neonatal radiculoneuropathy
R C Gilmartin, W Gooch, R S Wilroy, et al.
Clinical Genetics
|
April 1, 1977
Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases
A T Tharapel, R L Summitt, R S Wilroy, et al.
Annales De Genetique
|
December 1, 1977
Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family
R S Wilroy, R L Summitt, P Martens, et al.
Prenatal Diagnosis
|
January 1, 1986
Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counselling
A T Tharapel, J C Ward, L Wiggins, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)
|
August 1, 1983
Temporal bone findings in trisomy 13 with cyclopia
K Tomoda, J J Shea, R E Shenefelt, et al.
American Journal of Obstetrics and Gynecology
|
July 1, 1984
The concurrence of facioauriculovertebral spectrum and the Rokitansky syndrome
H T Winer-Muram, D Muram, R S Wilroy, et al.
Cancer Genetics and Cytogenetics
|
March 15, 1986
Philadelphia chromosome-positive chronic myelocytic leukemia with a supplementary t(4;9)(q21;p22) and long survival
S A Tharapel, G I Plitman, A T Tharapel, et al.
The Journal of Pediatrics
|
February 1, 1983
Anterior sacral defects: an autosomal dominantly inherited condition
V D Yates, R S Wilroy, G L Whitington, et al.
American Journal of Medical Genetics
|
October 1, 1991
High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement
M B Qumsiyeh, R S Wilroy, J N Peeden, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Pediatrics
|
March 1, 1979
Strychnine therapy in nonketotic hyperglycinemia
D Arneson, L T Ch'ien, P Chance, et al.
Birth Defects Original Article Series
|
January 1, 1977
Familial fatal neonatal radiculoneuropathy
R C Gilmartin, W Gooch, R S Wilroy, et al.
Clinical Genetics
|
April 1, 1977
Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases
A T Tharapel, R L Summitt, R S Wilroy, et al.
Annales De Genetique
|
December 1, 1977
Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family
R S Wilroy, R L Summitt, P Martens, et al.
Prenatal Diagnosis
|
January 1, 1986
Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counselling
A T Tharapel, J C Ward, L Wiggins, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)
|
August 1, 1983
Temporal bone findings in trisomy 13 with cyclopia
K Tomoda, J J Shea, R E Shenefelt, et al.
American Journal of Obstetrics and Gynecology
|
July 1, 1984
The concurrence of facioauriculovertebral spectrum and the Rokitansky syndrome
H T Winer-Muram, D Muram, R S Wilroy, et al.
Cancer Genetics and Cytogenetics
|
March 15, 1986
Philadelphia chromosome-positive chronic myelocytic leukemia with a supplementary t(4;9)(q21;p22) and long survival
S A Tharapel, G I Plitman, A T Tharapel, et al.
The Journal of Pediatrics
|
February 1, 1983
Anterior sacral defects: an autosomal dominantly inherited condition
V D Yates, R S Wilroy, G L Whitington, et al.
American Journal of Medical Genetics
|
October 1, 1991
High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement
M B Qumsiyeh, R S Wilroy, J N Peeden, et al.
Page
of 8