Search research articles
Contact Us
Filters
Showing results (11-20 of 28) with videos related to
Page
of 3
Sort By:
Clinical Genetics
|
January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance
M C Silengo, M Biagioli, G L Bell, et al.
Clinical and Experimental Dermatology
|
August 12, 2009
A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting
L Sorasio, E Biamino, E Garelli, et al.
Clinical Genetics
|
August 1, 1990
Heart-hand syndrome II. A report of Tabatznik syndrome with new findings
M C Silengo, M Biagioli, A Guala, et al.
American Journal of Medical Genetics
|
December 1, 1992
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasia
M Lerone, M Soliani, D Corea, et al.
Pediatric Radiology
|
January 1, 1990
A new syndrome with cerebro-oculo-skeletal-renal involvement
M C Silengo, M Lerone, A Pelizza, et al.
Clinical Genetics
|
February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new case
M Lerone, A Pessagno, A Taccone, et al.
Dermatology (Basel, Switzerland)
|
February 22, 2000
Total anonychia congenita in a woman with normal intelligence: report of a further case
M Priolo, L Rosaia, M Seri, et al.
Clinical Genetics
|
March 1, 1981
Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation
M C Silengo, L Luzzatti, W R Centerwall, et al.
American Journal of Medical Genetics
|
January 24, 1998
Ectodermal abnormalities in Kabuki syndrome
M Lerone, M Priolo, A Naselli, 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.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Clinical Genetics
|
January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance
M C Silengo, M Biagioli, G L Bell, et al.
Clinical and Experimental Dermatology
|
August 12, 2009
A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting
L Sorasio, E Biamino, E Garelli, et al.
Clinical Genetics
|
August 1, 1990
Heart-hand syndrome II. A report of Tabatznik syndrome with new findings
M C Silengo, M Biagioli, A Guala, et al.
American Journal of Medical Genetics
|
December 1, 1992
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasia
M Lerone, M Soliani, D Corea, et al.
Pediatric Radiology
|
January 1, 1990
A new syndrome with cerebro-oculo-skeletal-renal involvement
M C Silengo, M Lerone, A Pelizza, et al.
Clinical Genetics
|
February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new case
M Lerone, A Pessagno, A Taccone, et al.
Dermatology (Basel, Switzerland)
|
February 22, 2000
Total anonychia congenita in a woman with normal intelligence: report of a further case
M Priolo, L Rosaia, M Seri, et al.
Clinical Genetics
|
March 1, 1981
Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation
M C Silengo, L Luzzatti, W R Centerwall, et al.
American Journal of Medical Genetics
|
January 24, 1998
Ectodermal abnormalities in Kabuki syndrome
M Lerone, M Priolo, A Naselli, 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.
Page
of 3