B. Buldrini

New patients with Temple syndrome caused by 14q32 deletion: Genotype‐phenotype correlations and risk of thyroid cancer

L. Bernardini, A. Novelli, C. Graziano, 2016, American journal of medical genetics. Part A.

Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay

A. Ferlini, S. Fini, S. Bigoni, 2017, Molecular Syndromology.

Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis

E. Calzolari, A. Ferlini, P. Prontera, 2006, Prenatal diagnosis.

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q‐phenotype

S. Volinia, E. Calzolari, P. Prontera, 2008, American journal of medical genetics. Part A.

The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders

N. Nardocci, M. Eoli, S. Esposito, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic counseling for women referred for advanced maternal age: a telegenetic approach

A. Ferlini, M. Neri, L. Melchiorri, 2014, Genetics in Medicine.

A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature

A. Ferlini, S. Fini, S. Bigoni, 2018, Molecular Syndromology.

Paracentric inversion of Yq and review of the literature.

E. Calzolari, P. Prontera, A. Sensi, 2007, Genetic Counseling.

Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q).

A. Mencarelli, P. Prontera, E. Donti, 2010, Genetic counseling.

New patients with Temple syndrome caused by 14q32 deletion: Genotype‐phenotype correlations and risk of thyroid cancer

L. Bernardini, A. Novelli, C. Graziano, 2016, American journal of medical genetics. Part A.