Parental age in retinoblastoma

Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

Revue neurologique·2015

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

Placenta·2014

The presymptomatic phase of Huntington disease.

Revue neurologique·2012

[Critical approach to clinical trials: difficulties of such research in Lebanon].

Revue neurologique·2012

A one year prevalence study of schizophrenia on Reunion Island.

European psychiatry : the journal of the Association of European Psychiatrists·2009

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

Human mutation·2008

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Diagnostic performance of adult-based ultrasound ACR-TIRADS and C-TIRADS in adolescent thyroid nodules.

Frontiers in endocrinology·2026

Photo-based deep learning for detection of pediatric adenoid hypertrophy.

Digital health·2026

Associations of alexithymia, psychological problems, and emotion regulation difficulties with disordered eating behaviors in adolescents with type 1 diabetes.

Dusunen adam : Bakirkoy Ruh ve Sinir Hastaliklari Hastanesi yayin organi·2026

Pediatric thyroid cancer: a retrospective analysis of 42 cases.

Frontiers in oncology·2026

Novel Homozygous Mitochondrial Calcium Uptake Protein 1 Variant (c.38T>C, p.Leu13Pro) in a 7-year-old Girl with Congenital Ptosis and Proximal Myopathy: Expanding the Phenotypic Spectrum.

Annals of African medicine·2026

Child Opportunity Index and Suicide Risk Screening Positivity in Pediatric Emergency and Urgent Care Patients Presenting Without Behavioral Health Complaints.

Pediatric emergency care·2026

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Parental age in retinoblastoma

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Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

The presymptomatic phase of Huntington disease.

[Critical approach to clinical trials: difficulties of such research in Lebanon].

A one year prevalence study of schizophrenia on Reunion Island.

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Diagnostic performance of adult-based ultrasound ACR-TIRADS and C-TIRADS in adolescent thyroid nodules.

Photo-based deep learning for detection of pediatric adenoid hypertrophy.

Associations of alexithymia, psychological problems, and emotion regulation difficulties with disordered eating behaviors in adolescents with type 1 diabetes.

Pediatric thyroid cancer: a retrospective analysis of 42 cases.

Novel Homozygous Mitochondrial Calcium Uptake Protein 1 Variant (c.38T>C, p.Leu13Pro) in a 7-year-old Girl with Congenital Ptosis and Proximal Myopathy: Expanding the Phenotypic Spectrum.

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Parental age in retinoblastoma

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