Results 141 to 150 of about 4,709 (201)

Commentary: The Blue Whale [PDF]

, 1999
Liotta, P. H.
core   +1 more source

Epilepsy, EEG and chromosomal rearrangements. [PDF]

Epilepsia Open
Paprocka J, Coppola A, Cuccurullo C, Stawicka E, Striano P.   +4 more
europepmc   +1 more source

Facial Feminization Surgery: Preoperative Planning and Surgical Technique for a Harmonious Outcome.

Indian J Plast Surg, 2023
Asokan A, Sudheendran MK, Mohandas M, George PS, Nair RM.   +4 more
europepmc   +1 more source

A Model for Prediction of Propulsion Power and Emissions – Tankers and Bulk Carriers [PDF]

, 2012
Kristensen, Hans Otto Holmegaard, Lützen, Marie   +1 more
core  

Buffer Bulbous Bows: A Measure to Reduce Oil Spill in Collisions

, 2007
Formålet med denne afhandling at undersøge, hvor meget man ville kunne reducere olieudslip forårsaget af skibskollisioner ved at indføre mindre stærke bulbstævne på verdens skibe. Analysen omfatter såvel deterministiske som probabilistiske metoder. Afhandlingen består af et sammendrag og fem publikationer.
openaire  

Assessing cetacean encounter risk in offshore racing. [PDF]

Sci Rep
Virgili A, Fournier S, Le Maître O, Pocheau M, Ridoux V, Bañuls R.   +5 more
europepmc   +1 more source

A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity. [PDF]

Genes (Basel)
Cipriano L, Russo R, Andolfo I, Manno M, Piscopo R, Iolascon A, Piscopo C.   +6 more
europepmc   +1 more source

Anatomy, histology, and morphology of fish gills in relation to feeding habits: a comparative review of marine and freshwater species. [PDF]

BMC Zool
Alsafy MAM, Abd-Elhafeez HH, Rashwan AM, Erasha A, Ali S, El-Gendy SAA.   +5 more
europepmc   +1 more source

KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndrome. [PDF]

Hum Mol Genet
van Oirsouw ASE, Hadders MA, Koetsier M, Peters EDJ, Assia Batzir N, Barakat TS, Baralle D, Beil A, Bonnet-Dupeyron MN, Boone PM, Bouman A, Carere DA, Cogne B, Dunnington L, Farach LS, Genetti CA, Isidor B, Januel L, Joshi A, Lahiri N, Lee KN, Maya I, McEntagart M, Northrup H, Pujalte M, Richardson K, Walker S, Koeleman BPC, Alders M, van Jaarsveld RH, Oegema R.   +30 more
europepmc   +1 more source

Phenotypic and genotypic spectrum of noonan syndrome: A retrospective analysis of 46 consecutive pediatric patients presented at a regional cardiac center in China. [PDF]

Heliyon
Chen Q, Hong D, Huang Y, Zhang Z, Wang S.   +4 more
europepmc   +1 more source