Genetics in keratoconus: A, B, O blood groups

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

International journal of pediatric otorhinolaryngology·2008

Congenital anomaly rate in offspring of mothers with diabetes treated with insulin lispro during pregnancy.

Diabetic medicine : a journal of the British Diabetic Association·2005

Pre-gestational maternal body mass index predicts an increased risk of congenital malformations in infants of mothers with gestational diabetes.

Diabetic medicine : a journal of the British Diabetic Association·2005

Exstrophy of the cloaca and exstrophy of the bladder: two different expressions of a primary developmental field defect.

American journal of medical genetics·2001

Pathogenetic classification of a series of 27,145 consecutive infants with congenital defects.

American journal of medical genetics·2000

Maternal and fetal factors related to abnormal amniotic fluid.

Journal of perinatology : official journal of the California Perinatal Association·2000

Ocular toxicity of systemic chemotherapy with megadoses of carmustine and mitomycin.

Annals of ophthalmology·1994

Congenital intrastromal epithelial cyst of the iris.

Annals of ophthalmology·1994

Diagnosis and treatment of orbital hemorrhagic lesions.

Annals of ophthalmology·1994

The effect of gravity on the amplitude of accommodation.

Annals of ophthalmology·1994

Tuberculous choroiditis and acquired immunodeficiency syndrome.

Annals of ophthalmology·1994

Cataract extraction with lens implantation at Biloxi Veterans Affairs Medical Center: experience of ophthalmology residents.

Annals of ophthalmology·1994

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

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Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

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Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

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Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

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Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Diagnostics (Basel, Switzerland)·2026

Identification of the Novel HLA-DQB1*06:556 Allele by Next-Generation Sequencing.

HLA·2026

Related Experiment Videos

Genetics in keratoconus: A, B, O blood groups

Related Concept Videos

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

Congenital anomaly rate in offspring of mothers with diabetes treated with insulin lispro during pregnancy.

Pre-gestational maternal body mass index predicts an increased risk of congenital malformations in infants of mothers with gestational diabetes.

Exstrophy of the cloaca and exstrophy of the bladder: two different expressions of a primary developmental field defect.

Pathogenetic classification of a series of 27,145 consecutive infants with congenital defects.

Maternal and fetal factors related to abnormal amniotic fluid.

Ocular toxicity of systemic chemotherapy with megadoses of carmustine and mitomycin.

Congenital intrastromal epithelial cyst of the iris.

Diagnosis and treatment of orbital hemorrhagic lesions.

The effect of gravity on the amplitude of accommodation.

Tuberculous choroiditis and acquired immunodeficiency syndrome.

Cataract extraction with lens implantation at Biloxi Veterans Affairs Medical Center: experience of ophthalmology residents.

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Identification of the Novel HLA-DQB1*06:556 Allele by Next-Generation Sequencing.

Related Experiment Videos

Genetics in keratoconus: A, B, O blood groups

Abstract:

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