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American Journal of Medical Genetics
|
July 1, 1991
Trichothiodystrophy and ichthyosis as diagnostic signs
B G Kousseff
Pediatrics
|
September 1, 1986
Pleiotropy versus heterogeneity in Proteus syndrome
B G Kousseff
American Journal of Medical Genetics
|
July 1, 1992
Hypothesis: Jadassohn nevus phakomatosis: a paracrinopathy with variable phenotype
B G Kousseff
American Journal of Medical Genetics
|
February 1, 1984
Autosomal recessive spondylometepiphyseal dysplasia, type Strudwick
B G Kousseff, P Nichols
Birth Defects Original Article Series
|
January 1, 1985
A new autosomal recessive syndrome with Noonan-like phenotype, myopathy with congenital contractures and malignant hyperthermia
B G Kousseff, P Nichols
The Journal of Urology
|
April 1, 1984
Cryptorchidism in mental retardation
X Cortada, B G Kousseff
Birth Defects Original Article Series
|
January 1, 1982
The cytogenetic controversy regarding the Prader-Willi syndrome
B G Kousseff, R Douglass
The Journal of Pediatrics
|
April 1, 1981
Aniridia-Wilms tumor association
B G Kousseff, A Agatucci
Pediatric Neurology
|
April 1, 1995
Peripheral neuropathy in Ehlers-Danlos syndrome
E Galan, B G Kousseff
American Journal of Medical Genetics
|
December 1, 1990
Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII
J K Hartsfield, B G Kousseff
Page
of 10
Search research articles
Search
Showing results (21-30 of 93) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics
|
July 1, 1991
Trichothiodystrophy and ichthyosis as diagnostic signs
B G Kousseff
Pediatrics
|
September 1, 1986
Pleiotropy versus heterogeneity in Proteus syndrome
B G Kousseff
American Journal of Medical Genetics
|
July 1, 1992
Hypothesis: Jadassohn nevus phakomatosis: a paracrinopathy with variable phenotype
B G Kousseff
American Journal of Medical Genetics
|
February 1, 1984
Autosomal recessive spondylometepiphyseal dysplasia, type Strudwick
B G Kousseff, P Nichols
Birth Defects Original Article Series
|
January 1, 1985
A new autosomal recessive syndrome with Noonan-like phenotype, myopathy with congenital contractures and malignant hyperthermia
B G Kousseff, P Nichols
The Journal of Urology
|
April 1, 1984
Cryptorchidism in mental retardation
X Cortada, B G Kousseff
Birth Defects Original Article Series
|
January 1, 1982
The cytogenetic controversy regarding the Prader-Willi syndrome
B G Kousseff, R Douglass
The Journal of Pediatrics
|
April 1, 1981
Aniridia-Wilms tumor association
B G Kousseff, A Agatucci
Pediatric Neurology
|
April 1, 1995
Peripheral neuropathy in Ehlers-Danlos syndrome
E Galan, B G Kousseff
American Journal of Medical Genetics
|
December 1, 1990
Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII
J K Hartsfield, B G Kousseff
Page
of 10