Results 81 to 90 of about 3,407 (171)

Lithium ameliorates neural differentiation restoring cell death balance in Cornelia de Lange syndrome 2D and 3D models. [PDF]

Cell Death Discov
Parodi C, Lettieri A, Grazioli P, Di Fede E, Grassi S, Taci E, Toscani A, Prioni S, Rebellato S, Colombo EA, Rasetti S, Cutarelli A, Mariani M, Corti S, Finelli P, Prinetti A, Fazio G, Selicorni A, Conti L, Gervasini C, Massa V.   +20 more
europepmc   +1 more source

Clinical and genetic characteristics of Cornelia de Lange syndrome in pediatric patients. [PDF]

Pediatr Investig
Li X, Cheng M, Liu M, Li W, Li Y, Cao B, Wei L, Ding Y, Meng X, Li L, Gong C.   +10 more
europepmc   +1 more source

Cornelia de Lange syndrome. [PDF]

Journal of Medical Genetics, 1986
openaire   +2 more sources

A Complex Case of Langer-Giedion Syndrome, Cornelia de Lange Syndrome Type 4, and Hereditary Multiple Osteochondromas with Mosaic 8q23.1-q24.12 Deletion. [PDF]

Genes (Basel)
Valientes SDA, Wang H.
europepmc   +1 more source

A Rare Case of Coexisting 22q11.2 Deletion Syndrome and Cornelia De Lange Syndrome: A Case Report and Review of the Literature. [PDF]

Cureus
George E, Kontos K.
europepmc   +1 more source

Non-Classic Cornelia de Lange Syndrome Due to <i>BRD4</i> Gene Alterations: A Literature Review. [PDF]

Children (Basel)
Lonardo F, Falco M, Costabile C, Fontana P.   +3 more
europepmc   +1 more source

Overcoming diagnostic delays in Cornelia De Lange syndrome: the power of AI-driven genomics. [PDF]

Ann Med Surg (Lond)
Saleh Dahri S, Asadullah S, Talha M, Shamim L, Imran SB.   +4 more
europepmc   +1 more source

Evidence of spontaneous mentalizing in children with Cornelia de Lange and fragile X syndromes, but not autistic children. [PDF]

Oxf Open Neurosci
Ellis K, Moss J, Dziwisz M, Jones B, Griva C, Pendered S, Perry RC, White SJ.   +7 more
europepmc   +1 more source

Co-Occurrence of RAD21 and TNFAIP3 Mutations in Cornelia de Lange Syndrome with Pustular Psoriasis: Potential Molecular Interactions. [PDF]

Int J Mol Sci
Orozco BE, Orozco CV, Meléndez E, Mangones MF, Valderrama J, Lobato A, Garavito-Galofre P, Vélez JI, Vidal OM.   +8 more
europepmc   +1 more source

First description of co-occurrence of 49,XXXXY and X-linked Cornelia de Lange syndrome: case report. [PDF]

Front Endocrinol (Lausanne)
Al-Rashdi S, Ekstrom L, Collins A, Schulz HL, Dinwiddie A, Samango-Sprouse C, Olaya M, Moser E, Green AJ.   +8 more
europepmc   +1 more source