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Figure 1 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
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
I professionisti – Odontoiatria Saluzzese
Paolo Guanciali Franchi - Associate Professor - University of Chieti | LinkedIn
striscioni di “resistenza” in via Puccini - Pescara - Il Centro
Aneuploidy screening using circulating fetal cells in maternal blood by dual-probe FISH protocol: A prospective feasibility study on a series of 172 pregnant women
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
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
Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report | Journal of Medical Case Reports | Full Text
Nuovo ingresso femminile al Rotary Saluzzo della dott.ssa Tiziana Vavalà e relazione del socio Federico Guanciali Franchi – Rotary Club Saluzzo
A new case of mosaicism for invdup(15) duplicated for Prader–Willi/Angelman syndrome critical region (PWACR) in an adult healthy man - ScienceDirect
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
Volume 9, Issue 16 | Oncotarget
Frontiers | A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review | Endocrinology
PDF) Screening biochimici prenatali: l'eSperienza del tri-teSt in 17.869 gravidanze della regione abruzzo | Claudio Celentano - Academia.edu
Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report | Journal of Medical Case Reports | Full Text
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
il test sequenziale per lo screening della sindrome di ... - Mnlpublimed
Loop | Paolo Guanciali-Franchi
A G-banded chromosomes 8. B FISH analysis of the proband with the 8q24... | Download Scientific Diagram