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Journal of Genetic Disorders & Genetic Reports
Journal of Genetic Disorders & Genetic Reports
Department of Psychiatry University of Florida, USA
Verified email at omicsonline.org - Homepage
Title
Cited by
Cited by
Year
Ethical Implications in Genetic Counseling and Family Studies of the Epilepsies
B Godard
Journal of Genetic Disorders & Genetic Reports 11 (1), 2022
20*2022
Erring on the side of life: children with rare trisomy conditions, medical interventions and quality of life
D Bruns
J Genet Disord Genet Rep 1, 2, 2013
182013
Evaluation of genomic evidence for oxidative stress in experimental radiation nephropathy
EP Cohen, M Lenarczyk, BL Fish, S Jia, MJ Hessner, JE Moulder
Journal of genetic disorders & genetic reports 2 (1), 2013
142013
Genotype-phenotype characteristics of β thalassemia children in the Gaza Strip, Palestine
MM Yassin, MM Sirdah, RM Al Haddad, AH Lubbad, MS Al-Yazji
J Genet Disor Genet Rep 2 2, 2, 2013
122013
The Interpretation of Genetic Data-Considering the Effect of Changes to Gene Conformation-If the facts don’t support the theory, change the theory–how does this contribute to …
GW Ewing
J Genet Disor Genet Rep 6 4, 2, 2017
92017
Phenylketonuria (PKU) - What Next? Mini-Review
WB Hanley
Journal of Genetic Disorders & Genetic Reports 2 (2), 2013
72013
Left ventricular noncompaction in Noonan syndrome
RB Hinton, P Goldenberg, RC Godby, A Parrott, AG Shikany, BJ Landis, ...
J Genet Disor Genet Rep 5, 2, 2016
62016
Long-term follow-up of a patient with sitosterolemia and hemolytic anemia with excellent response to ezetimibe
A Quintás-Cardama, JJ McCarthy
Genet Disor Genet Rep 2, 1, 2013
62013
Ring14 international: development of a national-based patient association towards a “global” network initiative to fight a chromosomal disorder
S Azzali, Y DeWoody, B Rinaldi, M Crimi
J Genet Disor Genet Rep 4, 2, 2015
52015
Young Research Forum-Young Scientist Awards at Glycobiology 2020
A Heidari
J Genet Disor Genet Rep 8 (2), 2019
42019
Genotype and allele frequencies of calcium-sensing receptor gene a986s (rs1801725) polymorphism in Saudi adults
HS Sonbol, WF Al Otaibi
J. Genet. Disor. Genet. Rep 5 (3), 2016
42016
Telomeres in Cancer: Length, Positioning and Epigenetics
TN Patel, SR Nair, L Mohan, Y Fahmina, S AshwiniDevi
J Genet Disor Genet Rep 5 1, 2, 2016
42016
Fetuin A concentration in the amniotic fluid of fetuses with down syndrome
SB Kavak, EC Kavak, A Sen, R Ilhan, M Kaya, E Sapmaz, O Arat, ...
J Genet Disor Genet Rep 4 (1), 2015
42015
Lipoprotein Glomerulopathy: Molecular Characterization of Three Italian Patients and Literature Survey
S Bertolini, A Pasquariello, L Pisciotta, T Sampietro, G Pasquariello
J Genet Disor Genet Rep 3 1, 2, 2014
42014
Evidence that lithium inhibits export of N-acetyl-L-aspartate from neurons: A retrospective study of Canavan disease and bipolar disorder patients. A novel finding connecting …
MH Baslow, DN Guilfoyle
J Genet Disorders and Genet Reports 3 (1), 2014
42014
Molecular Genetic Testing for Carrier-Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1
K Renugadevi, JA Mary, V Perumalsamy, S Seshadri, S Jagadeesh, ...
J Genet Disor Genet Rep 3, 2, 2014
42014
Hereditary thrombocytosis in 3 Kuwaiti siblings with homozygous MPL Pro106Leu mutation and abnormal platelet aggregation
PR Marri, S Kirmani, V Rodriguez
J Genet Disor Genet Rep 2 (2), 10.4172, 2013
42013
Mini Review: HLA B27 and its Immunogenetics in Ankylosing Spondylitis
HN Tipu
J Genet Disor Genet Rep 2 1, 2, 2013
42013
Smith-Magenis syndrome treated with ramelteon and amphetamine-dextroamphetamine: case report and review of the literature
WS Baek, SH Elsea
J Genet Disor Genet Rep 5 4, 2, 2016
32016
Homozygous Point Mutation in a Patient with Spinal Muscular Atrophy Type 1
AVAG Isa Abdi Rad
Journal of Genetic Disorders & Genetic Reports 5 (3), 2016
32016
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