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Results of search for 'au:"MOLLICA, F"', page 6 of 7
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Authors
Antener, I
Bosco, P
Cavallaro, N
Di Bella, D
Di Martino, L
Distefano, G
Garozzo, R
Gorgone, G
Grasso, A
Incorpora, G
La Rosa, M
Li Volti, S
MOLLICA, F
Mattina, T
Mazzone, D
Mollica, F
Musumeci, S
Pavone, L
Russo, G
Sorge, G
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Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Female
Genes, Dominant
Humans
Infant
Infant, Newborn
Male
Pedigree
Pregnancy
Sicily
abnormalities
analysis
blood
complications
diagnosis
genetics
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Your search returned 137 results.
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101.
[Partial monosomy 9].
[electronic resource]
by
Pavone, L
Mollica, F
Sorge, G
Sciacca, F
d'Agata, A
Laurence, K M
Producer:
19791227
In:
Annales de genetique
vol. 21
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102.
Effect of polyamines on autohemolysis: studies on normal and thalassemic children.
[electronic resource]
by
Vanella, A
Rizza, V
Li Volti, S
Pinturo, R
Musumeci, S
Mollica, F
Producer:
19800923
In:
Acta haematologica
vol. 63
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103.
Increased erythrocytic spermine in Duchenne muscular dystrophy.
[electronic resource]
by
Mollica, F
Li Volti, S
Rapisarda, A
Longo, G
Pavone, L
Vanella, A
Producer:
19810327
In:
Pediatric research
vol. 14
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104.
Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosis.
[electronic resource]
by
Opitz, J M
Mollica, F
Sorge, G
Milana, G
Cimino, G
Caltabiano, M
Producer:
19940125
In:
American journal of medical genetics
vol. 47
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105.
Autosomal dominant atrial septal defect of ostium secundum type. Report of three families.
[electronic resource]
by
Li Volti, S
Distefano, G
Garozzo, R
Romeo, M G
Sciacca, P
Mollica, F
Producer:
19911204
In:
Annales de genetique
vol. 34
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106.
Acrofacial dysostosis of Nager and ocular abnormalities.
[electronic resource]
by
Pavone, L
Mollica, F
Pero, G
Tigano, G
Giancarlo, H
Mattucci, K
Setzen, M
Producer:
19870114
In:
Ophthalmic paediatrics and genetics
vol. 7
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107.
[Possibilities of the use of trans-intestinal intubation (end-to-end) for the study of the physiopathology of the gastrointestinal tract in infancy].
[electronic resource]
by
Di Martino, L
Mollica, F
Gula, G
La Rosa, M
Santonocito, B
Pisano, M
Producer:
19710823
In:
Bollettino della Societa italiana di biologia sperimentale
vol. 46
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108.
Imaging of urinary tract malformations: intravenous urography and/or kidney ultrasonography?
[electronic resource]
by
Li Volti, S
Di Bella, D
Garozzo, R
Di Fede, G F
Mollica, F
Producer:
19920206
In:
Child nephrology and urology
vol. 11
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109.
Familial optic atrophy with sex-influenced severity. A new variety of autosomal-dominant optic atrophy?
[electronic resource]
by
Gorgone, G
Li Volti, S
Cavallaro, N
Conti, L
Profeta, G M
Mollica, F
Producer:
19860530
In:
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde
vol. 192
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110.
Impaired antioxidant defense mechanisms in two children with hemolytic-uremic syndrome.
[electronic resource]
by
Li Volti, S
Di Giacomo, C
Garozzo, R
Campisi, A
Mollica, F
Vanella, A
Producer:
19931118
In:
Renal failure
vol. 15
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111.
Ocular manifestations in a family with probably X-linked cataracts.
[electronic resource]
by
Pavone, L
La Rosa, M
Sorge, G
Scaletta, S
Li Volti, S
Mollica, F
Producer:
19820521
In:
Clinical genetics
vol. 20
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112.
Sicily: a cluster of Hb G-San José.
[electronic resource]
by
Schilirò, G
Li Volti, S
Musumeci, S
Mollica, F
Marinucci, M
Mavilio, L
Tentori, L
Producer:
19820614
In:
Hemoglobin
vol. 5
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113.
Glucose-6-phosphate dehydrogenase deficiency and incidence of cataract in Sicily.
[electronic resource]
by
Moro, F
Gorgone, G
Li Volti, S
Cavallaro, N
Faro, S
Curreri, R
Mollica, F
Producer:
19851226
In:
Ophthalmic paediatrics and genetics
vol. 5
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114.
[Hemolytic disease of the newborn due to immunologic (ABO incompatibility excluded) and non-immunologic causes].
[electronic resource]
by
Gerbasi, M
Cutillo, S
Albeggiani, A
Balsamo, V
La Grutta, A
Mollica, F
Priolisi, A
Producer:
19690819
In:
Minerva pediatrica
vol. 19
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115.
Safety and effectiveness of an acellular pertussis vaccine in subjects with Down's syndrome.
[electronic resource]
by
Li Volti, S
Mattina, T
Mauro, L
Bianca, S
Anfuso, S
Ursino, A
Mollica, F
Producer:
19960815
In:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
vol. 12
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116.
Increase with age in the prevalence of beta-thalassemia trait among Sicilians.
[electronic resource]
by
Schiliro, G
Li Volti, S
Marino, S
Dibenedetto, S P
Samperi, P
Testa, R
Mollica, F
Producer:
19891005
In:
The New England journal of medicine
vol. 321
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117.
Hereditary twenty-nail dystrophy in a Sicilian family.
[electronic resource]
by
Pavone, L
Li Volti, S
Guarneri, B
La Rosa, M
Sorge, G
Incorpora, G
Mollica, F
Producer:
19830119
In:
Journal of medical genetics
vol. 19
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118.
Routine clinical application of the FRAXA Pfu PCR assay: limits and utility.
[electronic resource]
by
Condorelli, D F
Milana, G
Dell'Albani, P
Roccazzello, A M
Insirello, E
Pavone, L
Mollica, F
Producer:
19970325
In:
Clinical genetics
vol. 50
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119.
Hyporesponsiveness to intradermal administration of hepatitis B vaccine in insulin dependent diabetes mellitus.
[electronic resource]
by
Li Volti, S
Caruso-Nicoletti, M
Biazzo, F
Sciacca, A
Mandarà, G
Mancuso, M
Mollica, F
Producer:
19980422
In:
Archives of disease in childhood
vol. 78
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120.
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa.
[electronic resource]
by
Dunnill, M G
Richards, A J
Milana, G
Mollica, F
Eady, R A
Pope, F M
Producer:
19950228
In:
Human molecular genetics
vol. 3
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