Khaled R. Gaber

Giza, GZ, Egypt

Last Updated: 09/26/2026

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Found 13 publications

Evaluating microRNA-720 and microRNA-1275 as Noninvasive Specific Test Compared With Maternal Serum Alpha-Fetoprotein and Three-Dimensional Ultrasound to Diagnose Fetal Neural Tube Defects.

Evaluating microRNA-720 and microRNA-1275 as Noninvasive Specific Test Compared With Maternal Serum Alpha-Fetoprotein and Three-Dimensional Ultrasound to Diagnose Fetal Neural Tube Defects.

Journal: The journal of obstetrics and gynaecology research
Published: February 09, 2026

Prenatal diagnosis of mucopolysaccharidoses type II by two-dimensional electrophoresis and mass spectrometry in amniotic fluid.

Prenatal diagnosis of mucopolysaccharidoses type II by two-dimensional electrophoresis and mass spectrometry in amniotic fluid.

Journal: The journal of obstetrics and gynaecology research
Published: July 31, 2021

Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.

Genetic Implications in High-Risk Pregnancy and Its Outcome: A 2-Year Study.

Journal: American journal of perinatology
Published: February 26, 2021

Combination of Human Amniotic Fluid Derived-Mesenchymal Stem Cells and Nano-hydroxyapatite Scaffold Enhances Bone Regeneration.

Combination of Human Amniotic Fluid Derived-Mesenchymal Stem Cells and Nano-hydroxyapatite Scaffold Enhances Bone Regeneration.

Journal: Open access Macedonian journal of medical sciences
Published: August 06, 2019

Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families.

Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families.

Journal: BMC medical genomics
Published: June 05, 2019

Osteogenic Differentiation Potential of Human Bone Marrow and Amniotic Fluid-Derived Mesenchymal Stem Cells in Vitro & in Vivo.

Osteogenic Differentiation Potential of Human Bone Marrow and Amniotic Fluid-Derived Mesenchymal Stem Cells in Vitro & in Vivo.

Journal: Open access Macedonian journal of medical sciences
Published: December 05, 2018

Association between biomarkers of vitamin B12 status and the risk of neural tube defects.

Association between biomarkers of vitamin B12 status and the risk of neural tube defects.

Journal: The journal of obstetrics and gynaecology research
Published: March 23, 2018

Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.

Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.

Journal: American journal of medical genetics. Part A
Published: October 18, 2017

ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.

ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.

Journal: Genetic counseling (Geneva, Switzerland)
Published: January 01, 2016

Expanding the mutation and clinical spectrum of Roberts syndrome.

Expanding the mutation and clinical spectrum of Roberts syndrome.

Journal: Congenital anomalies
Published: June 13, 2015

Fetal brain disruption sequence versus fetal brain arrest: A distinct autosomal recessive developmental brain malformation phenotype.

Fetal brain disruption sequence versus fetal brain arrest: A distinct autosomal recessive developmental brain malformation phenotype.

Journal: American journal of medical genetics. Part A
Published: August 24, 2014

Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs).

Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs).

Journal: Gene
Published: March 18, 2012
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Last Updated: 09/26/2026