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Clinical and Experimental Rheumatology
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July 5, 2011
Chronic fatigue syndrome is commonly diagnosed in patients with Ehlers-Danlos syndrome hypermobility type/joint hypermobility syndrome
M Castori, C Celletti, F Camerota, et al.
Pathologica
|
January 1, 1983
[X-linked familial pituitary nanism]
C Di Fusco, M Baldi, P Grammatico, et al.
Minerva Ginecologica
|
January 1, 1986
[Complex balanced translation]
G Del Porto, P Grammatico, M Baldi, et al.
Tissue Antigens
|
December 21, 2013
Detection of a novel HLA-B allele, HLA-B*08:111, in an Italian bone marrow donor
C Barzi, C Vecchiato, M Catalano, et al.
The American Journal of Dermatopathology
|
April 1, 1996
Granulomatous slack skin. Report of a case and review of the literature
L Balus, L Manente, D Remotti, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
Attention-deficit/hyperactivity disorder, speech delay and polymicrogyria associated with trisomy 18 mosaicism
R Rinaldi, P Parisi, M Poscente, et al.
Journal of Medical Genetics
|
October 1, 1984
Familial centric fission of chromosome 4
G Del Porto, C Di Fusco, M Baldi, et al.
Clinical Genetics
|
June 1, 1992
20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome
P Grammatico, F Cupilari, C Di Rosa, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
Del(4)(pter-->q33:) case report and review of the literature
P Grammatico, L Spaccini, C Di Rosa, et al.
Annales De Genetique
|
January 1, 1994
First case of deletion 14q11.2q13: clinical phenotype
P Grammatico, S de Sanctis, C di Rosa, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Clinical and Experimental Rheumatology
|
July 5, 2011
Chronic fatigue syndrome is commonly diagnosed in patients with Ehlers-Danlos syndrome hypermobility type/joint hypermobility syndrome
M Castori, C Celletti, F Camerota, et al.
Pathologica
|
January 1, 1983
[X-linked familial pituitary nanism]
C Di Fusco, M Baldi, P Grammatico, et al.
Minerva Ginecologica
|
January 1, 1986
[Complex balanced translation]
G Del Porto, P Grammatico, M Baldi, et al.
Tissue Antigens
|
December 21, 2013
Detection of a novel HLA-B allele, HLA-B*08:111, in an Italian bone marrow donor
C Barzi, C Vecchiato, M Catalano, et al.
The American Journal of Dermatopathology
|
April 1, 1996
Granulomatous slack skin. Report of a case and review of the literature
L Balus, L Manente, D Remotti, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
Attention-deficit/hyperactivity disorder, speech delay and polymicrogyria associated with trisomy 18 mosaicism
R Rinaldi, P Parisi, M Poscente, et al.
Journal of Medical Genetics
|
October 1, 1984
Familial centric fission of chromosome 4
G Del Porto, C Di Fusco, M Baldi, et al.
Clinical Genetics
|
June 1, 1992
20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome
P Grammatico, F Cupilari, C Di Rosa, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
Del(4)(pter-->q33:) case report and review of the literature
P Grammatico, L Spaccini, C Di Rosa, et al.
Annales De Genetique
|
January 1, 1994
First case of deletion 14q11.2q13: clinical phenotype
P Grammatico, S de Sanctis, C di Rosa, et al.
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of 7