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Paolo Guanciali Franchi - Associate Professor - University of Chieti |  LinkedIn
Paolo Guanciali Franchi - Associate Professor - University of Chieti | LinkedIn

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a  case report | Journal of Medical Case Reports | Full Text
Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report | Journal of Medical Case Reports | Full Text

Loop | Paolo Guanciali-Franchi
Loop | Paolo Guanciali-Franchi

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a  case report | Journal of Medical Case Reports | Full Text
Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report | Journal of Medical Case Reports | Full Text

Cancers | Free Full-Text | HNRNPL Restrains miR-155 Targeting of BUB1 to  Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic  Leukemia
Cancers | Free Full-Text | HNRNPL Restrains miR-155 Targeting of BUB1 to Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic Leukemia

Nuovo ingresso femminile al Rotary Saluzzo della dott.ssa Tiziana Vavalà e  relazione del socio Federico Guanciali Franchi – Rotary Club Saluzzo
Nuovo ingresso femminile al Rotary Saluzzo della dott.ssa Tiziana Vavalà e relazione del socio Federico Guanciali Franchi – Rotary Club Saluzzo

Cancers | Free Full-Text | HNRNPL Restrains miR-155 Targeting of BUB1 to  Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic  Leukemia
Cancers | Free Full-Text | HNRNPL Restrains miR-155 Targeting of BUB1 to Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic Leukemia

Paolo Guanciali-Franchi's research works | Università degli Studi G.  d'Annunzio Chieti e Pescara, Chieti (UNICH) and other places
Paolo Guanciali-Franchi's research works | Università degli Studi G. d'Annunzio Chieti e Pescara, Chieti (UNICH) and other places

Microduplications of 22q11.2 are frequently inherited and are associated  with variable phenotypes | Genetics in Medicine
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes | Genetics in Medicine

Sequential combined test, second trimester maternal serum markers, and  circulating fetal cells to select women for invasive prenatal diagnosis |  PLOS ONE
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis | PLOS ONE

Biologia e microbiologia Prof. R. Piccolomini
Biologia e microbiologia Prof. R. Piccolomini

Establishment and functions of DNA methylation in the germline | Epigenomics
Establishment and functions of DNA methylation in the germline | Epigenomics

A new case of mosaicism for invdup(15) duplicated for Prader–Willi/Angelman  syndrome critical region (PWACR) in an adult healthy man - ScienceDirect
A new case of mosaicism for invdup(15) duplicated for Prader–Willi/Angelman syndrome critical region (PWACR) in an adult healthy man - ScienceDirect

Cancers | Free Full-Text | HNRNPL Restrains miR-155 Targeting of BUB1 to  Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic  Leukemia
Cancers | Free Full-Text | HNRNPL Restrains miR-155 Targeting of BUB1 to Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic Leukemia

Case report of newborn with de novo partial trisomy 2q31.2–37.3 and  monosomy 9p24.3 | SpringerLink
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 | SpringerLink

Figure 2 from A new case of mosaicism for invdup(15) duplicated for  Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy  man. | Semantic Scholar
Figure 2 from A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. | Semantic Scholar

Sequential combined test, second trimester maternal serum markers, and  circulating fetal cells to select women for invasive prenatal diagnosis |  PLOS ONE
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis | PLOS ONE

Clinical and molecular diagnosis, screening and management of  Beckwith–Wiedemann syndrome: an international consensus statement | Nature  Reviews Endocrinology
Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement | Nature Reviews Endocrinology

PDF) Cystic hygroma and mid-trimester maternal serum screening | Federico  Prefumo - Academia.edu
PDF) Cystic hygroma and mid-trimester maternal serum screening | Federico Prefumo - Academia.edu

GUANCIALI FRANCHI Paolo Emilio | Università degli Studi "G. d'Annunzio"  Chieti - Pescara
GUANCIALI FRANCHI Paolo Emilio | Università degli Studi "G. d'Annunzio" Chieti - Pescara

HNRNPL Restrains <i>miR-155</i> Targeting of BUB1 to Stabilize Aberrant  Karyotypes of Transformed Cells in Chronic Lymphocytic Leukemia. - Abstract  - Europe PMC
HNRNPL Restrains <i>miR-155</i> Targeting of BUB1 to Stabilize Aberrant Karyotypes of Transformed Cells in Chronic Lymphocytic Leukemia. - Abstract - Europe PMC

PDF) Screening biochimici prenatali: l'eSperienza del tri-teSt in 17.869  gravidanze della regione abruzzo | Claudio Celentano - Academia.edu
PDF) Screening biochimici prenatali: l'eSperienza del tri-teSt in 17.869 gravidanze della regione abruzzo | Claudio Celentano - Academia.edu

I professionisti – Odontoiatria Saluzzese
I professionisti – Odontoiatria Saluzzese