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Annales De Genetique
|
January 1, 1991
Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and review
L Zelante, F Torricelli, S Calvano, et al.
American Journal of Medical Genetics
|
December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and son
A Giannotti, M C Digilio, R Mingarelli, et al.
Clinical Genetics
|
September 1, 1995
Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IV
M C Digilio, A Giannotti, G Pagnotta, et al.
Clinical Dysmorphology
|
October 1, 1995
Sporadic trichodental dysplasia with microcephaly and mental retardation
A Giannotti, M C Digilio, G Albertini, et al.
Skeletal Radiology
|
July 7, 2005
Quantitative ultrasound of the hand phalanges in a cohort of monozygotic twins: influence of genetic and environmental factors
G Guglielmi, F de Terlizzi, I Torrente, et al.
Prenatal Diagnosis
|
December 1, 1994
Fetal detection of dup 9p11-12
G Calabrese, L Stuppia, P Guanciali-Franchi, et al.
Giornale Italiano Di Cardiologia
|
February 1, 1994
[Genetics of congenital heart diseases]
B Dallapiccola, R Mingarelli, M C Digilio, et al.
Journal of the American College of Cardiology
|
May 20, 1999
Guidelines for 22q11 deletion screening of patients with conotruncal defects
M C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics
|
July 31, 1995
Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome
M C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics
|
November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype
A Giannotti, M C Digilio, B Marino, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 84) with videos related to
Sort By:
Page
of 9
Annales De Genetique
|
January 1, 1991
Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and review
L Zelante, F Torricelli, S Calvano, et al.
American Journal of Medical Genetics
|
December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and son
A Giannotti, M C Digilio, R Mingarelli, et al.
Clinical Genetics
|
September 1, 1995
Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IV
M C Digilio, A Giannotti, G Pagnotta, et al.
Clinical Dysmorphology
|
October 1, 1995
Sporadic trichodental dysplasia with microcephaly and mental retardation
A Giannotti, M C Digilio, G Albertini, et al.
Skeletal Radiology
|
July 7, 2005
Quantitative ultrasound of the hand phalanges in a cohort of monozygotic twins: influence of genetic and environmental factors
G Guglielmi, F de Terlizzi, I Torrente, et al.
Prenatal Diagnosis
|
December 1, 1994
Fetal detection of dup 9p11-12
G Calabrese, L Stuppia, P Guanciali-Franchi, et al.
Giornale Italiano Di Cardiologia
|
February 1, 1994
[Genetics of congenital heart diseases]
B Dallapiccola, R Mingarelli, M C Digilio, et al.
Journal of the American College of Cardiology
|
May 20, 1999
Guidelines for 22q11 deletion screening of patients with conotruncal defects
M C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics
|
July 31, 1995
Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome
M C Digilio, B Marino, A Giannotti, et al.
American Journal of Medical Genetics
|
November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype
A Giannotti, M C Digilio, B Marino, et al.
Page
of 9