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Results of search for 'au:"MOLLICA, F"', page 5 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
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Child, Preschool
Female
Genes, Dominant
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Infant, Newborn
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Pedigree
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abnormalities
analysis
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Your search returned 137 results.
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81.
Haematological studies in a case of oculocerebrorenal syndrome.
[electronic resource]
by
Pavone, L
Musumeci, S
Li Volti, S
Distefano, G
Mollica, F
Producer:
19770611
In:
Helvetica paediatrica acta
vol. 31
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82.
Convergence of two types of familial short stature in a pedigree.
[electronic resource]
by
Mollica, F
Li Volti, S
Pavone, L
Vigo, R
Raiti, S
Producer:
19810915
In:
Acta endocrinologica
vol. 97
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83.
Serum IgE in polytransfused thalassemic patients.
[electronic resource]
by
La Rosa, M
Pavone, L
Musumeci, S
Mollica, F
Ronchetti, R
Producer:
19831220
In:
Vox sanguinis
vol. 45
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84.
Farber's lipogranulomatosis: ceramidase deficiency and prolonged survival in three relatives.
[electronic resource]
by
Pavone, L
Moser, H W
Mollica, F
Reitano, C
Durand, P
Producer:
19810224
In:
The Johns Hopkins medical journal
vol. 147
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85.
Asymmetric crying facies and congenital eye defects in an infant.
[electronic resource]
by
Pavone, L
Mollica, F
La Rosa, M
Borellini, S
Bianchine, J W
Producer:
19780828
In:
Acta paediatrica Belgica
vol. 31
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86.
Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.
[electronic resource]
by
Gangarossa, S
Mattina, T
Romano, V
Milana, G
Mollica, F
Schilirò, G
Producer:
19961213
In:
American journal of medical genetics
vol. 62
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87.
Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion.
[electronic resource]
by
Gangarossa, S
Schiliró, G
Mattina, T
Scardilli, S
Mollica, F
Cavallari, V
Producer:
19960718
In:
Blood
vol. 87
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88.
Treatment of infantile spasms with sodium dipropylacetic acid.
[electronic resource]
by
Pavone, L
Incorpora, G
La Rosa, M
Li Volti, S
Mollica, F
Producer:
19811122
In:
Developmental medicine and child neurology
vol. 23
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89.
[Neurological and muscular manifestations of thalassemia major (author's transl)].
[electronic resource]
by
Mollica, F
Romeo, M A
di Gregorio, F
Grasso, A
Pavone, L
Producer:
19810413
In:
Archives francaises de pediatrie
vol. 37
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90.
Antley-Bixler syndrome.
[electronic resource]
by
Mattina, T
Pierluigi, M
Perfumo, C
Mazzone, D
Scardilli, S
Mollica, F
Producer:
19970326
In:
Clinical genetics
vol. 50
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91.
Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.
[electronic resource]
by
Mattina, T
Pierluigi, M
Mazzone, D
Scardilli, S
Perfumo, C
Mollica, F
Producer:
19980130
In:
Journal of medical genetics
vol. 34
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92.
Serum IgE in newborns undergoing exchange transfusion.
[electronic resource]
by
La Rosa, M
Romeo, M G
Pratico, G
Rizzo, R
Mollica, F
Producer:
19861113
In:
Annals of allergy
vol. 57
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93.
Acute post-streptococcal glomerulonephritis in an 8-month-old girl.
[electronic resource]
by
Li Volti, S
Furnari, M L
Garozzo, R
Santangelo, G
Mollica, F
Producer:
19940421
In:
Pediatric nephrology (Berlin, Germany)
vol. 7
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94.
Wolfram's syndrome and HLA.
[electronic resource]
by
Mattina, T
Li Volti, S
Palmeri, P
Tribulato, A
Salerno, A
Mollica, F
Producer:
19880922
In:
Ophthalmic paediatrics and genetics
vol. 9
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95.
[Intrafamilial variation in congenital ophthalmoplegia: studies in a Sicilian family].
[electronic resource]
by
Mollica, F
Li Volti, S
Incorpora, G
Tita, F
Tomarchio, S
Moro, F
Producer:
19801024
In:
Journal de genetique humaine
vol. 28
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96.
Autosomal dominant cone-rod dystrophy associated with sickle-cell trait in a Sicilian family.
[electronic resource]
by
Gorgone, G
Li Volti, S
Tomarchio, S
Pavone, L
Profeta, G
Mollica, F
Producer:
19860609
In:
Ophthalmic paediatrics and genetics
vol. 7
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97.
Autosomal dominant cataract and microcornea associated with myopia in a Sicilian family.
[electronic resource]
by
Mollica, F
Li Volti, S
Tomarchio, S
Gangi, A
Risiglione, V
Gorgone, G
Producer:
19851021
In:
Clinical genetics
vol. 28
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98.
Dextrocardia with and without situs viscerum inversus in two sibs.
[electronic resource]
by
Distefano, G
Romeo, M G
Grasso, S
Mazzone, D
Sciacca, P
Mollica, F
Producer:
19880128
In:
American journal of medical genetics
vol. 27
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99.
[A further case of monosomy 9p].
[electronic resource]
by
Pavone, L
Mollica, F
Sorge, G
Sciacca, F
D'Agata, A
Laurence, K M
Producer:
19800923
In:
Pathologica
vol. 71
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100.
Congenital obstruction of the lacrimal passages in five consecutive generations.
[electronic resource]
by
Moro, F
Li Volti, S
Tomarchio, S
Pavone, L
Martorina, M
Mollica, F
Producer:
19810709
In:
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde
vol. 181
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