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Archives of Dermatology
|
December 1, 1995
Tuberous sclerosis. The persistent challenge of clinical diagnosis
R E Schnur
Seminars in Cutaneous Medicine and Surgery
|
March 1, 1997
Reticulate hyperpigmentation
R E Schnur, W R Heymann
Human Genetics
|
May 1, 1995
Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS)
R E Schnur, P A Wick
Journal of Youth and Adolescence
|
November 27, 2013
Stages of identity development and problem drinking in college women
R E Schnur, M L Macdonald
American Journal of Medical Genetics
|
March 17, 1997
Circumferential ringed creases ("Michelin tire babies") with specific histologic findings and/or karyotype abnormalities: clues to molecular pathogenesis?
R E Schnur, E H Zackai
Pediatric Dermatology
|
March 1, 1994
Buschke-Ollendorff syndrome, otosclerosis, and congenital spinal stenosis
R E Schnur, K Grace, A Herzberg
American Journal of Medical Genetics
|
September 1, 1987
Thrombocytopenia with absent radius in a boy and his uncle
R E Schnur, D L Eunpu, E H Zackai
Archives of Dermatology
|
June 30, 1998
Clustered angiofibromas on the ear of a patient with neurofibromatosis type 2
A T Jaffe, W R Heymann, R E Schnur
American Journal of Medical Genetics
|
May 2, 1997
Utility of linked markers in genetic counseling: estimation of carrier risks in X-linked ocular albinism
T R Rebbeck, H A Jordan, R E Schnur, et al.
Neuroradiology
|
July 1, 1997
Magnetization transfer in the investigation of patients with tuberous sclerosis
N Girard, R A Zimmerman, R E Schnur, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Archives of Dermatology
|
December 1, 1995
Tuberous sclerosis. The persistent challenge of clinical diagnosis
R E Schnur
Seminars in Cutaneous Medicine and Surgery
|
March 1, 1997
Reticulate hyperpigmentation
R E Schnur, W R Heymann
Human Genetics
|
May 1, 1995
Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS)
R E Schnur, P A Wick
Journal of Youth and Adolescence
|
November 27, 2013
Stages of identity development and problem drinking in college women
R E Schnur, M L Macdonald
American Journal of Medical Genetics
|
March 17, 1997
Circumferential ringed creases ("Michelin tire babies") with specific histologic findings and/or karyotype abnormalities: clues to molecular pathogenesis?
R E Schnur, E H Zackai
Pediatric Dermatology
|
March 1, 1994
Buschke-Ollendorff syndrome, otosclerosis, and congenital spinal stenosis
R E Schnur, K Grace, A Herzberg
American Journal of Medical Genetics
|
September 1, 1987
Thrombocytopenia with absent radius in a boy and his uncle
R E Schnur, D L Eunpu, E H Zackai
Archives of Dermatology
|
June 30, 1998
Clustered angiofibromas on the ear of a patient with neurofibromatosis type 2
A T Jaffe, W R Heymann, R E Schnur
American Journal of Medical Genetics
|
May 2, 1997
Utility of linked markers in genetic counseling: estimation of carrier risks in X-linked ocular albinism
T R Rebbeck, H A Jordan, R E Schnur, et al.
Neuroradiology
|
July 1, 1997
Magnetization transfer in the investigation of patients with tuberous sclerosis
N Girard, R A Zimmerman, R E Schnur, et al.
Page
of 4