A
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Abd El-Fattah, Safa N.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
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Abdel Kader, Rania M.
Cytogenetic and Clinical Description of Maternally Inherited Pure Trisomy 4p [Volume 13, Issue 1, 2024, Pages 16-20]
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Abdel Kader, Rania M.A.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
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Abd-Elnaby, Azza E
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
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Abdelrahman, Amany H.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
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Abdel Salam, Ghada M.H.
Cytogenetic and Clinical Description of Maternally Inherited Pure Trisomy 4p [Volume 13, Issue 1, 2024, Pages 16-20]
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Aglan, Mona S.
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate Syndrome (EEC) in Patients with TP63 Variants [Volume 13, Issue 1, 2024, Pages 9-15]
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Ashaat, Engy A.
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
B
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Behiry, Eman Gamal
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
E
-
Eid, Maha M.
Cytogenetic and Clinical Description of Maternally Inherited Pure Trisomy 4p [Volume 13, Issue 1, 2024, Pages 16-20]
-
Eid, Maha M.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
-
Eid, Ola M.
Cytogenetic and Clinical Description of Maternally Inherited Pure Trisomy 4p [Volume 13, Issue 1, 2024, Pages 16-20]
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Eid, Ola M.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
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Eid, Ola M.
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
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Eissa, Noura R.
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate Syndrome (EEC) in Patients with TP63 Variants [Volume 13, Issue 1, 2024, Pages 9-15]
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Elaidy, Aya
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
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El Gazzar, Mohammed Abd Elmaboud
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
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El-kholey, Weaam Mohammed Mohammed
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
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Elshaer, Osama Saad
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
-
Esmail, Asmaa M.
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate Syndrome (EEC) in Patients with TP63 Variants [Volume 13, Issue 1, 2024, Pages 9-15]
-
Essawi, Mona L.
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate Syndrome (EEC) in Patients with TP63 Variants [Volume 13, Issue 1, 2024, Pages 9-15]
F
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Fahiem, Reham Ahmed
Genetic Predisposition of Language Disorders Among Different Independent Factors in Bronchial Asthma [Volume 13, Issue 1, 2024, Pages 32-38]
-
Farid, Marwa
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
H
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Hassan, Heba Amin
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate Syndrome (EEC) in Patients with TP63 Variants [Volume 13, Issue 1, 2024, Pages 9-15]
-
Hussein, Fatma
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
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Hussen, Dalia Farouk
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
I
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Issa, Hesham Ali
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
K
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Kamel, Alaa K
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
M
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Mahrous, Rana
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
-
Mazen, Inas M.
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
-
Meguid, Nagwa A.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
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Mekkawy, Mona K.
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
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Mohamed, Amal M.
Hot spots copy number variations, 15q methylation, and SHANK3 single nucleotide polymorphisms study in a group of Egyptian Autistic children [Volume 13, Issue 1, 2024, Pages 21-31]
R
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Ramadan, Abeer
Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4) Gene Variants in Females with Recurrent Spontaneous Pregnancy Loss [Volume 13, Issue 1, 2024, Pages 1-8]
-
Refaee, Abdelrahman Shawky
Genetic Predisposition of Language Disorders Among Different Independent Factors in Bronchial Asthma [Volume 13, Issue 1, 2024, Pages 32-38]
S
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Sayed, Shereen A.
Copy Number Variation Study of A Cohort of 46,XY DSD Patients [Volume 13, Issue 1, 2024, Pages 39-49]
-
Sayed-Ahmed, Mohammed Mamdouh
Genetic Predisposition of Language Disorders Among Different Independent Factors in Bronchial Asthma [Volume 13, Issue 1, 2024, Pages 32-38]
T
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Temtamy, Samia A.
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate Syndrome (EEC) in Patients with TP63 Variants [Volume 13, Issue 1, 2024, Pages 9-15]
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