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Clinical Genetics
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May 1, 1984
Abnormal B.A.E.P. in a family with Moebius syndrome: evidence for supranuclear lesion
M Stabile, M L Cavaliere, G Scarano, et al.
American Journal of Medical Genetics
|
August 1, 1989
CFC syndrome: report on three additional cases
G Sorge, F Di Forti, G Scarano, et al.
Birth Defects Original Article Series
|
January 1, 1996
A case of short-rib syndrome without polydactyly in a stillborn: a new type?
G Scarano, M Della Monica, G Capece, et al.
Clinical Genetics
|
March 1, 1994
Cerebro-facio-articular syndrome of Van Maldergem: confirmation of a new MR/MCA syndrome
G Zampino, C Colosimo, F Balducci, et al.
Clinical Genetics
|
September 1, 2017
Say-Barber-Biesecker-Young-Simpson syndrome and Genitopatellar syndrome: Lumping or splitting?
F Lonardo, M S Lonardo, F Acquaviva, et al.
Biochimica Et Biophysica Acta
|
March 7, 1996
Archaeal elongation factor 1 beta is a dimer. Primary structure, molecular and biochemical properties
G Raimo, M Masullo, G Savino, et al.
Human Reproduction (Oxford, England)
|
September 9, 2006
WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report
A Biason-Lauber, G De Filippo, D Konrad, et al.
Annales De Genetique
|
January 1, 1982
t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome
B Dallapiccola, I Bianco, V Brinchi, et al.
Birth Defects Original Article Series
|
January 1, 1996
Malformation syndromes with kidney dysplasia
M Genuardi, G Scarano, C Tozzi, et al.
Human Mutation
|
January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta
M Mottes, M M Gomez Lira, M Valli, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
Clinical Genetics
|
May 1, 1984
Abnormal B.A.E.P. in a family with Moebius syndrome: evidence for supranuclear lesion
M Stabile, M L Cavaliere, G Scarano, et al.
American Journal of Medical Genetics
|
August 1, 1989
CFC syndrome: report on three additional cases
G Sorge, F Di Forti, G Scarano, et al.
Birth Defects Original Article Series
|
January 1, 1996
A case of short-rib syndrome without polydactyly in a stillborn: a new type?
G Scarano, M Della Monica, G Capece, et al.
Clinical Genetics
|
March 1, 1994
Cerebro-facio-articular syndrome of Van Maldergem: confirmation of a new MR/MCA syndrome
G Zampino, C Colosimo, F Balducci, et al.
Clinical Genetics
|
September 1, 2017
Say-Barber-Biesecker-Young-Simpson syndrome and Genitopatellar syndrome: Lumping or splitting?
F Lonardo, M S Lonardo, F Acquaviva, et al.
Biochimica Et Biophysica Acta
|
March 7, 1996
Archaeal elongation factor 1 beta is a dimer. Primary structure, molecular and biochemical properties
G Raimo, M Masullo, G Savino, et al.
Human Reproduction (Oxford, England)
|
September 9, 2006
WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report
A Biason-Lauber, G De Filippo, D Konrad, et al.
Annales De Genetique
|
January 1, 1982
t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome
B Dallapiccola, I Bianco, V Brinchi, et al.
Birth Defects Original Article Series
|
January 1, 1996
Malformation syndromes with kidney dysplasia
M Genuardi, G Scarano, C Tozzi, et al.
Human Mutation
|
January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta
M Mottes, M M Gomez Lira, M Valli, et al.
Page
of 7