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Ophthalmic Paediatrics and Genetics
|
August 1, 1986
'Leopard spot' retinopathy in Warburg syndrome
R A Barth, R A Pagon, A H Bunt-Milam
The Journal of Pediatrics
|
April 6, 1999
Phenotypic spectrum and management issues in Kabuki syndrome
H Kawame, M C Hannibal, L Hudgins, et al.
Investigative Ophthalmology & Visual Science
|
April 1, 1983
Clinical-ultrastructural study of a retinal dystrophy
A H Bunt-Milam, R E Kalina, R A Pagon
Human Genetics
|
January 1, 1984
X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes
C M Disteche, K Swisshelm, S Forbes, et al.
Journal of Medical Genetics
|
August 1, 1985
Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder
R A Pagon, T D Bird, J C Detter, et al.
Gastroenterology
|
April 1, 1988
Visceral myopathy of the gastrointestinal and genitourinary tracts in infants
M D Schuffler, R A Pagon, R Schwartz, et al.
Developmental Medicine and Child Neurology
|
April 1, 1996
Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three children
J F McLaughlin, R A Pagon, E Weinberger, et al.
American Journal of Medical Genetics
|
March 3, 1997
Facio-oculo-acoustico-renal (FOAR) syndrome: case report and review
D B Schowalter, R A Pagon, R E Kalina, et al.
Developmental Medicine and Child Neurology
|
July 1, 1996
Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three children
J F McLaughlin, R A Pagon, E Weinberger, et al.
The Journal of Pediatrics
|
August 1, 1981
Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association
R A Pagon, J M Graham, J Zonana, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 104) with videos related to
Sort By:
Page
of 11
Ophthalmic Paediatrics and Genetics
|
August 1, 1986
'Leopard spot' retinopathy in Warburg syndrome
R A Barth, R A Pagon, A H Bunt-Milam
The Journal of Pediatrics
|
April 6, 1999
Phenotypic spectrum and management issues in Kabuki syndrome
H Kawame, M C Hannibal, L Hudgins, et al.
Investigative Ophthalmology & Visual Science
|
April 1, 1983
Clinical-ultrastructural study of a retinal dystrophy
A H Bunt-Milam, R E Kalina, R A Pagon
Human Genetics
|
January 1, 1984
X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes
C M Disteche, K Swisshelm, S Forbes, et al.
Journal of Medical Genetics
|
August 1, 1985
Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder
R A Pagon, T D Bird, J C Detter, et al.
Gastroenterology
|
April 1, 1988
Visceral myopathy of the gastrointestinal and genitourinary tracts in infants
M D Schuffler, R A Pagon, R Schwartz, et al.
Developmental Medicine and Child Neurology
|
April 1, 1996
Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three children
J F McLaughlin, R A Pagon, E Weinberger, et al.
American Journal of Medical Genetics
|
March 3, 1997
Facio-oculo-acoustico-renal (FOAR) syndrome: case report and review
D B Schowalter, R A Pagon, R E Kalina, et al.
Developmental Medicine and Child Neurology
|
July 1, 1996
Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three children
J F McLaughlin, R A Pagon, E Weinberger, et al.
The Journal of Pediatrics
|
August 1, 1981
Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association
R A Pagon, J M Graham, J Zonana, et al.
Page
of 11