Results 61 to 70 of about 63,159 (270)

Morphology of Guard Hairs in Amazonian Marsupials: Intergeneric Variation, Habitat and Habit Association in a Phylogenetic Framework of the Order Didelphimorphia

Acta Zoologica, EarlyView.
ABSTRACT The cuticle and medulla of guard hairs exhibit distinct morphological patterns among mammalian species. To investigate this variability in marsupials from the Brazilian Amazon, we analysed guard hairs from nine Didelphimorphia species and incorporated data from an additional 25 didelphid species.
Matheus M. Bitencourt, Ana Cristina Mendes‐Oliveira, Gleomar F. Maschio, Maria Clara S. Ribeiro, Alexandra M. R. Bezerra   +4 more
wiley   +1 more source

Genetica molecolare della fibrosi cistica

, 1997
Dottorato di ricerca in genetica umana. 6. ciclo. A.a. 1995-96. Coordinatore A. O. Carbonara. Tutore A. CarbonaraConsiglio Nazionale delle Ricerche - Biblioteca Centrale - P.le Aldo Moro, 7, Rome; Biblioteca Nazionale Centrale - P.za Cavalleggeri, 1 ...
Garnerone, Simonetta
core  

Geometric Morphometrics Reveal Body Shape Variation in Freshwater Shrimps of the Genus Macrobrachium Lacking a Mandibular Palp (Formerly Pseudopalaemon Sollaud, 1911) (Decapoda: Palaemonidae)

Acta Zoologica, EarlyView.
ABSTRACT Shape variation in the cephalothorax of Macrobrachium species without mandibular palp using geometric morphometrics was used as a tool to support species differentiation and propose new diagnostic characters for taxonomic identification.
Thaís Arrais Mota, Ana Carla Soares da Silva, Lucas Jhones de Santana Neves, Carlos Eduardo Rocha Duarte Alencar, Fabrício Lopes Carvalho   +4 more
wiley   +1 more source

CAPITOLO 10. LA GENETICA GENERALE ED UMANA

, 2008
CAPITOLO DEDICATO ALLA GENETICA MENDELIANA E GENETICA MOLECOLARE ...
TOGNON, Mauro
core  

Filologia e genetica.

Cuadernos de Filología Italiana, 1996
Sin ...
Giuseppe Tavani
doaj  

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

Molecular Genetics & Genomic Medicine, 2020
Background Chromosomal microarray analysis (CMA) is nowadays widely used in the diagnostic path of patients with clinical phenotypes. However, there is no ascertained evidence to date on how to assemble single/combined clinical categories of ...
Ilaria Catusi, Maria Paola Recalcati, Ilaria Bestetti, Maria Garzo, Chiara Valtorta, Melissa Alfonsi, Alberta Alghisi, Stefania Cappellani, Rosario Casalone, Rossella Caselli, Caterina Ceccarini, Carlo Ceglia, Anna Maria Ciaschini, Domenico Coviello, Francesca Crosti, Annamaria D'Aprile, Antonella Fabretto, Rita Genesio, Marzia Giagnacovo, Paola Granata, Ilaria Longo, Michela Malacarne, Giuseppina Marseglia, Annamaria Montaldi, Anna Maria Nardone, Chiara Palka, Vanna Pecile, Chiara Pessina, Diana Postorivo, Serena Redaelli, Alessandra Renieri, Chiara Rigon, Fabiola Tiberi, Mariella Tonelli, Nicoletta Villa, Anna Zilio, Daniela Zuccarello, Antonio Novelli, Lidia Larizza, Daniela Giardino   +39 more
doaj   +1 more source

Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants

Clinical Genetics, EarlyView.
SEMA6A plays a role in cell migration and axon guidance in the developing central nervous system. Phenotypes seen in eleven individuals heterozygous for SEMA6A variants included developmental delay, intellectual disability, autism/autistic behaviors, behavioral abnormalities, attention disorders, hypotonia, and brain anomalies.
Evan Burchfiel, Xiaonan Zhao, Nichole M. Owen, Tia Gordon, Mahshid S. Azamian, Eric C. Kao, Fan Xia, Xi Luo, Jill A. Rosenfeld, Seema R. Lalani, Allison P. Ortega, Steven B. Bleyl, Florence Petit, Sulekha Rajagopolan, Bénédicte Demeer, Meredith K. Gillespie, Lijia Huang, Matthew Osmond, Kym M. Boycott, Kyra E. Stuurman, Marjon A. van Slegtenhorst, Haley Soller, Céline Jost, Aurore Garde, Hana Safraou, Laurence Faivre, Victor Faundes, Daryl A. Scott   +27 more
wiley   +1 more source

Aspetti medico legali nell'attività di Genetica Medica

, 2014
Le frontiere sempre più ampie della genetica medica, soprattutto nel settore della diagnostica prenatale, hanno visto espandersi il profilo del rischio per il professionista e per la struttura nella quale opera.
R. Zoja
core  

GENETICA GENERALE

, 2020
Genetica formale Metodo e prove sperimentali di Mendel Caratteri singoli e segregazione, Caratteri e assortimento indipendente, Esperienze mendeliane "ieri ed oggi", I Leggi di Mendel, I Caratteri mendeliani e reincrocio IGenetica "oltre ...
FASANO,S, TOGNON,M, BARISANI,D, DE LEO,G, DI BELLA,MA, MENEVERI,R   +5 more
core  

Liability to Chromosome Damage in Lymphocytes of “Cancer Family” Subjects: A Study of Spontaneous and Induced Chromosomal Fragility

The International Journal of Biological Markers, 1987
Spontaneous chromosomal fragility was detected in seven tumor patients and one healthy member from two families with a high recurrence of cancer. Major chromosome lesions, such as terminal deletions and rearranged chromosomes, were found at levels ...
Lidia Larizza, Luisa Doneda, Miria Stefanini, Giuseppa Francone, Valter Gualandri, Annamaria Fuhrman Conti   +5 more
doaj   +1 more source