Dermatoglyphics in gonadal dysgenesis: analysis of palmar patients

Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population.

HLA·2016

Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2015

One-year clinical evaluation of a Glass Carbomer fissure sealant, a preliminary study.

The European journal of prosthodontics and restorative dentistry·2014

Influence of ultrasonic excitation and heat application on the microleakage of glass ionomer cements.

Australian dental journal·2012

4''-O-(omega-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens.

Bioorganic & medicinal chemistry·2010

Characteristics of the craniofacial complex in Turner syndrome.

Archives of oral biology·2009

[Psychodynamic aspects of criminal behavior].

Acta medica Iugoslavica·1991

The functioning of personality and the success of group psychotherapy of alcoholics.

Acta medica Iugoslavica·1991

Thoracocentesis under ultrasonographic control.

Acta medica Iugoslavica·1991

[The frequency of urinary tract infections in hospitalized infants].

Acta medica Iugoslavica·1991

[Mortality in malignant hemopathies in Yugoslavia].

Acta medica Iugoslavica·1991

[Implantation of intraocular lenses in patients with diabetes].

Acta medica Iugoslavica·1991

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Molecular biology and evolution·2026

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Brain communications·2026

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Brain, behavior, and immunity·2026

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

Legal medicine (Tokyo, Japan)·2026

LINE-1 repeats are a defining feature of the Xce.

Proceedings of the National Academy of Sciences of the United States of America·2026

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

JCI insight·2026

Related Experiment Videos

Dermatoglyphics in gonadal dysgenesis: analysis of palmar patients

Related Concept Videos

Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population.

Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.

One-year clinical evaluation of a Glass Carbomer fissure sealant, a preliminary study.

Influence of ultrasonic excitation and heat application on the microleakage of glass ionomer cements.

4''-O-(omega-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens.

Characteristics of the craniofacial complex in Turner syndrome.

[Psychodynamic aspects of criminal behavior].

The functioning of personality and the success of group psychotherapy of alcoholics.

Thoracocentesis under ultrasonographic control.

[The frequency of urinary tract infections in hospitalized infants].

[Mortality in malignant hemopathies in Yugoslavia].

[Implantation of intraocular lenses in patients with diabetes].

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

LINE-1 repeats are a defining feature of the Xce.

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

Related Experiment Videos

Dermatoglyphics in gonadal dysgenesis: analysis of palmar patients

Related Concept Videos

Related Articles