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Results of search for 'au:"MOLLICA, F"', page 2 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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21.
[The alkali-resistant hemoglobin level in thalassemia major in relation to age, sex and the principal hematological characteristics].
[electronic resource]
by
LA GRUTTA, A
MOLLICA, F
Producer:
19981101
In:
La Pediatria
vol. 67
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22.
Should all children receive two measles vaccinations?
[electronic resource]
by
Li Volti, S
Mollica, F
Producer:
19931022
In:
Clinical pediatrics
vol. 32
Online resources:
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23.
Trisomy 22 mosaicism.
[electronic resource]
by
Mollica, F
Sorge, G
Pavone, L
Producer:
19770917
In:
Journal of medical genetics
vol. 14
Online resources:
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24.
Maternal drug ingestion and cyclopia.
[electronic resource]
by
Mollica, F
Pavone, L
Sorge, G
Producer:
19810521
In:
The Journal of pediatrics
vol. 98
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25.
Linear sebaceous nevus syndrome in a newborn.
[electronic resource]
by
Mollica, F
Pavone, L
Nuciforo, G
Producer:
19750310
In:
American journal of diseases of children (1960)
vol. 128
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26.
[Translocation mongolism (presentation of a family with 14/21 translocation)].
[electronic resource]
by
Sorge, G
Garozzo, R
Mollica, F
Producer:
19780218
In:
La Pediatria
vol. 85
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27.
Neonatal hepatitis in five children of a hepatitis B surface antigen carrier woman.
[electronic resource]
by
Mollica, F
Musumeci, S
Fischer, A
Producer:
19770630
In:
The Journal of pediatrics
vol. 90
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28.
Familial hyperprolinemia without mental retardation and hereditary nephropathy.
[electronic resource]
by
Mollica, F
Pavone, L
Antener, I
Producer:
19730904
In:
Monographs in human genetics
vol. 6
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29.
Short stature, mental retardation and ocular alterations in three siblings.
[electronic resource]
by
Mollica, F
Pavone, L
Antener, I
Producer:
19730215
In:
Helvetica paediatrica acta
vol. 27
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30.
Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
[electronic resource]
by
Mollica, F
Pavone, L
Antener, I
Producer:
19710929
In:
Pediatrics
vol. 48
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31.
HbsAb content in commercial immunoglobins.
[electronic resource]
by
Mollica, F
Musumeci, S
Fischer, A
Producer:
19810827
In:
Annali Sclavo; rivista di microbiologia e di immunologia
vol. 22
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32.
[Congenital hereditary corneal dystrophy associated with various extraoculary anomalies].
[electronic resource]
by
Scialfa, A
Mollica, F
Pavone, L
Producer:
19751223
In:
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde
vol. 171
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33.
Autosomal recessive postaxial polydactyly type A in a Sicilian family.
[electronic resource]
by
Mollica, F
Volti, S L
Sorge, G
Producer:
19780929
In:
Journal of medical genetics
vol. 15
Online resources:
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34.
[In vivo study of the electric activity of the colon in childhood].
[electronic resource]
by
Di Martino, L
Gula, G
Mollica, F
Producer:
19720801
In:
La Pediatria
vol. 80
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35.
[Research on cytochemical methods of demonstration of erythrocytic glucose-6-phosphate dehydrogenase].
[electronic resource]
by
Mollica, F
Pavone, L
Di Stefano, G
Producer:
19700225
In:
La Pediatria
vol. 77
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36.
New syndrome: exostoses, anetodermia, brachydactyly.
[electronic resource]
by
Mollica, F
Li Volti, S
Guarneri, B
Producer:
19850205
In:
American journal of medical genetics
vol. 19
Online resources:
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37.
Hemolysis in typhoid fever.
[electronic resource]
by
La Grutta, A
Balsamo, V
Mollica, F
Producer:
19670529
In:
British medical journal
vol. 2
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38.
Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs.
[electronic resource]
by
Pavone, L
Mollica, F
Levy, H L
Producer:
19760226
In:
Archives of disease in childhood
vol. 50
Online resources:
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39.
Prenatal diagnosis of thalassemia: the viewpoint of patients.
[electronic resource]
by
Schilirò, G
Romeo, M A
Mollica, F
Producer:
19880701
In:
Prenatal diagnosis
vol. 8
Online resources:
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40.
[Congenital non-bullous ichthyosiforme erythroderma. Two brothers with a particularly severe form].
[electronic resource]
by
Mollica, F
Romeo, M A
Pavone, L
Producer:
20060120
In:
Annales de pediatrie
vol. 24
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