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American Journal of Medical Genetics
|
May 15, 1993
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease
P Franceschini, M P Vardeu, F Signorile, et al.
Annales De Dermatologie Et De Venereologie
|
January 1, 1981
[Lupus, insulin-resistant diabetes and acanthosis nigricans (author's transl)]
B Wechsler, J P Michel, D Molle, et al.
Human Genetics
|
November 16, 1978
Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter)
P Franceschini, M C Silengo, G F Davi, et al.
American Journal of Medical Genetics
|
August 17, 1999
Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and review
P Franceschini, D Licata, G Di Cara, et al.
Clinical Genetics
|
February 1, 1984
The Neu-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case
M C Silengo, G Davi, R Bianco, et al.
La Radiologia Medica
|
July 11, 1992
[The preoperative staging of rectal cancer with endorectal echography]
L Franceschini, D Mascagni, F Gobbi, et al.
Clinical Genetics
|
May 1, 1982
Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndrome
M C Silengo, G F Davi, R Bianco, et al.
Clinical Genetics
|
June 1, 1984
Interstitial deletion of chromosome 1 (q23-q25). Report of a case
M C Silengo, G F Davi, R Bianco, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
November 1, 2013
In an elite cross of maize a major quantitative trait locus controls one-fourth of the genetic variation for grain yield
P Ajnone-Marsan, G Monfredini, W F Ludwig, et al.
Minerva Pediatrica
|
March 31, 1982
[The Freeman-Sheldon syndrome with mental retardation]
M Cirillo Silengo, G F Davi, R Bianco, et al.
Page
of 13
Search research articles
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Showing results (101-110 of 130) with videos related to
Sort By:
Page
of 13
American Journal of Medical Genetics
|
May 15, 1993
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease
P Franceschini, M P Vardeu, F Signorile, et al.
Annales De Dermatologie Et De Venereologie
|
January 1, 1981
[Lupus, insulin-resistant diabetes and acanthosis nigricans (author's transl)]
B Wechsler, J P Michel, D Molle, et al.
Human Genetics
|
November 16, 1978
Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter)
P Franceschini, M C Silengo, G F Davi, et al.
American Journal of Medical Genetics
|
August 17, 1999
Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and review
P Franceschini, D Licata, G Di Cara, et al.
Clinical Genetics
|
February 1, 1984
The Neu-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case
M C Silengo, G Davi, R Bianco, et al.
La Radiologia Medica
|
July 11, 1992
[The preoperative staging of rectal cancer with endorectal echography]
L Franceschini, D Mascagni, F Gobbi, et al.
Clinical Genetics
|
May 1, 1982
Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndrome
M C Silengo, G F Davi, R Bianco, et al.
Clinical Genetics
|
June 1, 1984
Interstitial deletion of chromosome 1 (q23-q25). Report of a case
M C Silengo, G F Davi, R Bianco, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
November 1, 2013
In an elite cross of maize a major quantitative trait locus controls one-fourth of the genetic variation for grain yield
P Ajnone-Marsan, G Monfredini, W F Ludwig, et al.
Minerva Pediatrica
|
March 31, 1982
[The Freeman-Sheldon syndrome with mental retardation]
M Cirillo Silengo, G F Davi, R Bianco, et al.
Page
of 13