Results 41 to 50 of about 2,385 (150)

Estimation rapide du taux de germination de l'arachide [PDF]

open access: yes, 1993
Les méthodes de contrôle de la valeur semencière des graines d'arachide, pratiquées par les laboratoires spécialisés répondent soit aux normes très élaborées de l'International Seed Testing Association (ISTA), soit aux différentes méthodes ou ...
Schilling, Robert
core  

A Comparative Study of Masanumasik Garbha Vikas Krama according to Ayurveda with Its Clinical Importance [PDF]

open access: yes, 2021
In universe human is the best creation of Nature. It is a miracle and wonder of the nature which have proper shape, size and weight of human body. Procuring a baby is a lifetime dream of every female in the society.
Arvind Kumar Yadav   +3 more
core   +1 more source

Ajo selenizado: ¿un alimento funcional futuro o actual? [PDF]

open access: yes, 2012
In the last years, functional foods have awakened consumer, scientific and business interest. A commonly found vegetable in such kind of foods includes garlic (Allium sativum).
Escudero, Leticia B.   +4 more
core  

Nail patella syndrome: a rare cause of renal failure in a young adult [PDF]

open access: yes, 2011
Nail Patella Syndrome (NPS) is a rare hereditary disease affecting multiple systems with predominant involvement of Kidney, Bones and Nails and Eyes. We report a case of NPS which presented as renal failure in a 22 year old male. The patient was admitted
Senguttuvan, NB   +3 more
core   +2 more sources

Non-Mosaic Tetrasomy 9p in An Infant With Multiple Congenital Anomalies

open access: yesGynecology Obstetrics & Reproductive Medicine, 2007
Supernumerary isochromosomes resulting in autosomal tetrasomy are rare and have been described for 12p, 18p and 9p. To date, approximately 30 patients have been described with a tetrasomy 9p, majority of cases being mosaics.
Füsun Düzcan   +5 more
doaj  

Zimmermann-Laband syndrome : clinical and cytogenetic study in two related patients [PDF]

open access: yes, 2019
Zimmermann?Laband Syndrome (ZLS) is an extremely rare autosomal dominant congenital disorder. It is a craniofacial malformation syndrome with predominant intraoral involvement consisting of gingival fibromatosis diffusion in early development.
Daneshbod, Khosrow   +6 more
core   +2 more sources

Mechanisms and molecular regulation of mammalian tooth replacement [PDF]

open access: yes, 2008
In most non-mammalian vertebrates, such as fish and reptiles, teeth are replaced continuously. However, tooth replacement in most mammals, including human, takes place only once and further renewal is apparently inhibited.
Järvinen, Elina
core  

Severe Ocular Surface abnormalities in a child and Ectodermal Dysplasia: A Case Report. [PDF]

open access: yes, 2019
Ectodermal Dysplasia is a disorder that occurs due to abnormal development of at least two major ectodermal derivatives in the developing embryo. Author report the case of a 10 year old male child who was referred to our department with complaints of ...
Minhas, Shailender   +2 more
core   +2 more sources

Typically Unobserved Variables (TUVs) and Selection into Prenatal Inputs: Implications for Estimating Infant Health Production Functions [PDF]

open access: yes
We examine the extent to which infant health production functions are sensitive to model specification and measurement error. We focus on the importance of typically unobserved but theoretically important variables (TUVs), other non-standard covariates ...
Dhaval Dave   +3 more
core  

Distinctive phenotypic abnormalities associated with submicroscopic 21q22 deletion including DYRK1A [PDF]

open access: yes, 2010
Partial monosomy 21 has been reported, but the phenotypes described are variable with location and size of the deletion. We present 2 patients with a partially overlapping microdeletion of 21q22 and a striking phenotypic resemblance.
Coo, I.F.M. (René) de   +16 more
core  

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