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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1991
[Hypophosphatasia: a family study]
A Guala, P Tomà, M E Liverani, et al.
Clinical Genetics
|
July 25, 2000
Psychomotor development in Cri du Chat Syndrome
P Cerruti Mainardi, A Guala, G Pastore, et al.
Minerva Pediatrica
|
September 15, 1985
[Epidemiological study on the incidence of malignant tumors in children in the province of Vercelli in the years 1975-1979]
P Cerruti-Mainardi, G Colombino, R Colombo, et al.
Minerva Pediatrica
|
October 31, 1985
[Investigation on the frequency of 3 congenital malformations in newborn infants in the Vercelli province in the years 1975-1979]
P Cerruti Mainardi, A Ziliotto, M E Liverani, et al.
Minerva Cardioangiologica
|
July 1, 1985
[Application of dynamic electrocardiography in neonatal cardiological evaluation. I. Heart rhythm and rate in the first 24 hours of life of the preterm infant]
P L Roncarolo, G Cossa, E Vercellotti, et al.
Minerva Pediatrica
|
June 26, 2012
[The Cri du Chat syndrome: a study on the quality of care]
P Cerruti Mainardi, M Spunton, V Arcuri, et al.
Journal of Medical Genetics
|
February 24, 2001
The first three mosaic cri du chat syndrome patients with two rearranged cell lines
C Perfumo, P Cerruti Mainardi, A Calí, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1997
[Malformations of the midline. A case-control study]
A Guala, G Pastore, P Cerruti Mainardi, et al.
Hormone Research
|
May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review
L Garavelli, P Cerruti-Mainardi, R Virdis, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature
L Garavelli, M Zollino, P Cerruti Mainardi, et al.
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of 2
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1991
[Hypophosphatasia: a family study]
A Guala, P Tomà, M E Liverani, et al.
Clinical Genetics
|
July 25, 2000
Psychomotor development in Cri du Chat Syndrome
P Cerruti Mainardi, A Guala, G Pastore, et al.
Minerva Pediatrica
|
September 15, 1985
[Epidemiological study on the incidence of malignant tumors in children in the province of Vercelli in the years 1975-1979]
P Cerruti-Mainardi, G Colombino, R Colombo, et al.
Minerva Pediatrica
|
October 31, 1985
[Investigation on the frequency of 3 congenital malformations in newborn infants in the Vercelli province in the years 1975-1979]
P Cerruti Mainardi, A Ziliotto, M E Liverani, et al.
Minerva Cardioangiologica
|
July 1, 1985
[Application of dynamic electrocardiography in neonatal cardiological evaluation. I. Heart rhythm and rate in the first 24 hours of life of the preterm infant]
P L Roncarolo, G Cossa, E Vercellotti, et al.
Minerva Pediatrica
|
June 26, 2012
[The Cri du Chat syndrome: a study on the quality of care]
P Cerruti Mainardi, M Spunton, V Arcuri, et al.
Journal of Medical Genetics
|
February 24, 2001
The first three mosaic cri du chat syndrome patients with two rearranged cell lines
C Perfumo, P Cerruti Mainardi, A Calí, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1997
[Malformations of the midline. A case-control study]
A Guala, G Pastore, P Cerruti Mainardi, et al.
Hormone Research
|
May 24, 2005
Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review
L Garavelli, P Cerruti-Mainardi, R Virdis, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature
L Garavelli, M Zollino, P Cerruti Mainardi, et al.
Page
of 2