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1.
Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia.
Genes Chromosomes Cancer
; 60(2): 79-87, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33135230
2.
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Am J Hum Genet
; 97(6): 869-77, 2015 Dec 03.
Article
in English
| MEDLINE | ID: mdl-26608785
3.
Human sperm aneuploidy after exposure to polycyclic aromatic hydrocarbons.
Reprod Fertil Dev
; 2015 Mar 10.
Article
in English
| MEDLINE | ID: mdl-25751082
4.
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.
Brain Sci
; 14(3)2024 Mar 13.
Article
in English
| MEDLINE | ID: mdl-38539661
5.
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.
Circ Cardiovasc Genet
; 10(5)2017 Oct.
Article
in English
| MEDLINE | ID: mdl-29025761
6.
The association between environmental exposure to pyrethroids and sperm aneuploidy.
Chemosphere
; 128: 42-8, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25655817
7.
Lifestyle factors and sperm aneuploidy.
Reprod Biol
; 14(3): 190-9, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-25152516
8.
Human urinary phthalate metabolites level and main semen parameters, sperm chromatin structure, sperm aneuploidy and reproductive hormones.
Reprod Toxicol
; 42: 232-41, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-24140385
9.
Large deletion in the KAL1 gene in two related patients with hypogonadotropic hypogonadism: diagnostic usefulness of cytogenetic and molecular methods.
Endokrynol Pol
; 62(3): 224-9, 2011.
Article
in English
| MEDLINE | ID: mdl-21717404
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