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Journal of Medical Genetics
|
May 1, 1993
ICF syndrome with variable expression in sibs
G Gimelli, P Varone, A Pezzolo, et al.
Hemoglobin
|
January 7, 1998
Hb Siirt [beta 27(B9)Ala-->Gly]: a new, electrophoretically silent, hemoglobin variant
I Bianco, M P Cappabianca, M Lerone, et al.
Minerva Pediatrica
|
March 1, 1991
[Identification of the dystrophin gene deletions in DMD/BMD patients. Analysis of the reading frame shift and germinal mosaicism]
A E Covone, F Caroli, A Cereseto, et al.
Birth Defects Original Article Series
|
January 1, 1982
Thalassemia types in Latium
I Bianco, B Graziani, M Lerone, et al.
American Journal of Medical Genetics
|
November 1, 1993
Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly: report of a new patient with additional findings
M Silengo, M Lerone, G Romeo, 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.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 1, 1990
[Lip pits and Van der Woude syndrome. Description of a new familial case]
A Rizzo, M Lerone, G Martucciello, et al.
American Journal of Medical Genetics
|
January 24, 1998
Ectodermal abnormalities in Kabuki syndrome
M Lerone, M Priolo, A Naselli, 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.
Page
of 7
Search research articles
Search
Showing results (11-20 of 70) with videos related to
Sort By:
Page
of 7
Journal of Medical Genetics
|
May 1, 1993
ICF syndrome with variable expression in sibs
G Gimelli, P Varone, A Pezzolo, et al.
Hemoglobin
|
January 7, 1998
Hb Siirt [beta 27(B9)Ala-->Gly]: a new, electrophoretically silent, hemoglobin variant
I Bianco, M P Cappabianca, M Lerone, et al.
Minerva Pediatrica
|
March 1, 1991
[Identification of the dystrophin gene deletions in DMD/BMD patients. Analysis of the reading frame shift and germinal mosaicism]
A E Covone, F Caroli, A Cereseto, et al.
Birth Defects Original Article Series
|
January 1, 1982
Thalassemia types in Latium
I Bianco, B Graziani, M Lerone, et al.
American Journal of Medical Genetics
|
November 1, 1993
Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly: report of a new patient with additional findings
M Silengo, M Lerone, G Romeo, 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.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
January 1, 1990
[Lip pits and Van der Woude syndrome. Description of a new familial case]
A Rizzo, M Lerone, G Martucciello, et al.
American Journal of Medical Genetics
|
January 24, 1998
Ectodermal abnormalities in Kabuki syndrome
M Lerone, M Priolo, A Naselli, 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.
Page
of 7