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Journal of Medical Genetics
|
August 1, 1980
Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family
G Morelli, C Mesolella, M L Cavaliere, et al.
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.
Journal of Medical Genetics
|
October 1, 1980
Primary protrusio acetabuli in four generations of an Italian family
V Ventruto, M Stabile, M L Cavaliere, et al.
Minerva Pediatrica
|
June 15, 1980
[A case of Poland's syndrome. Brachysyndactyly and deficiency of the pectoralis major muscle]
M Stabile, R Pisciotta, M L Cavaliere, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1997
Phenotypic variability in the chromosome 9 ring
M L Cavaliere, M M Rinaldi, P Castelluccio, et al.
Clinical Genetics
|
November 1, 1980
A and B postaxial polydactyly in two members of the same family
V Ventruto, G Theo, A Celona, et al.
La Radiologia Medica
|
March 1, 1981
[XXXXY syndrome: clinical-radiological findings in one patient (author's transl)]
V Ventruto, R Pisciotta, A Celona, et al.
Journal of Medical Genetics
|
June 1, 1984
Ring (13),t(2;6) associated with familial fragile (16)
V Ventruto, A Rinaldi, S Renda, et al.
FEBS Letters
|
August 10, 2000
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)
A Orrico, L Galli, M Falciani, et al.
American Journal of Medical Genetics
|
December 1, 1983
Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13)
V Ventruto, R Pisciotta, S Renda, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Journal of Medical Genetics
|
August 1, 1980
Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family
G Morelli, C Mesolella, M L Cavaliere, et al.
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.
Journal of Medical Genetics
|
October 1, 1980
Primary protrusio acetabuli in four generations of an Italian family
V Ventruto, M Stabile, M L Cavaliere, et al.
Minerva Pediatrica
|
June 15, 1980
[A case of Poland's syndrome. Brachysyndactyly and deficiency of the pectoralis major muscle]
M Stabile, R Pisciotta, M L Cavaliere, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1997
Phenotypic variability in the chromosome 9 ring
M L Cavaliere, M M Rinaldi, P Castelluccio, et al.
Clinical Genetics
|
November 1, 1980
A and B postaxial polydactyly in two members of the same family
V Ventruto, G Theo, A Celona, et al.
La Radiologia Medica
|
March 1, 1981
[XXXXY syndrome: clinical-radiological findings in one patient (author's transl)]
V Ventruto, R Pisciotta, A Celona, et al.
Journal of Medical Genetics
|
June 1, 1984
Ring (13),t(2;6) associated with familial fragile (16)
V Ventruto, A Rinaldi, S Renda, et al.
FEBS Letters
|
August 10, 2000
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)
A Orrico, L Galli, M Falciani, et al.
American Journal of Medical Genetics
|
December 1, 1983
Multiple skeletal familial abnormalities associated with balanced reciprocal translocation 2;8(q32;p13)
V Ventruto, R Pisciotta, S Renda, et al.
Page
of 2