L. Dain
发表
A. Nadra,
Carlos D Bruque,
Jorge E Kolomenski,
2020,
Human mutation.
L. Dain,
G. Alonso,
T. Pasqualini,
2013,
Archivos argentinos de pediatria.
M. Vazquez-Levin,
J. Biancotti,
L. Dain,
2003,
Fertility and sterility.
M. Rittler,
V. Cosentino,
M. Delea,
2018,
Genes.
L. Dain,
G. Alonso,
T. Pasqualini,
2007,
Medicina.
P. Ghiringhelli,
L. Espeche,
Melisa Taboas,
2015,
Endocrine.
L. Dain,
M. Escobar,
V. Chiauzzi,
2004,
Molecular and Cellular Endocrinology.
A. Nadra,
M. Delea,
L. Espeche,
2016,
Scientific Reports.
Javier Santos,
A. Nadra,
C. Paván,
2020,
Scientific Reports.
L. Dain,
José María Sánchez,
C. P. Kaminker,
1985,
American journal of medical genetics.
A. Berenstein,
M. Rittler,
V. Cosentino,
2020,
Genes.
P. Lapunzina,
J. Nevado,
R. Armando,
2020,
Molecular Biology Reports.
A. Nadra,
Jorge E Kolomenski,
M. Delea,
2018,
Human mutation.
Expression of fragile X mental retardation protein and Fmr1 mRNA during folliculogenesis in the rat.
M. Tesone,
F. Parborell,
L. Dain,
2013,
Reproduction.
S. Belli,
M. Delea,
L. Espeche,
2017,
Genes.
N. Ceballos,
Melisa Taboas,
L. Dain,
2014,
PloS one.
Alejandro D. Nadra,
A. Nadra,
S. Belli,
2011,
PloS one.
S. Campo,
L. Dain,
L. Andreone,
2006
.
P. Validire,
A. Rajkovic,
E. Rajpert-De Meyts,
2018,
Human molecular genetics.
S. Belli,
Jorge E Kolomenski,
M. Delea,
2020,
Clinical endocrinology.
M. Rittler,
M. Delea,
L. Dain,
2019,
Clinical dysmorphology.
Javier Santos,
A. Nadra,
M. F. Pignataro,
2019,
Sub-cellular biochemistry.
M. Delea,
L. Espeche,
L. Dain,
2019,
Cytogenetic and Genome Research.
S. Campo,
L. Dain,
L. Andreone,
2006,
Human reproduction.
Isolated p.H62L Mutation in the CYP21A2 Gene in a Simple Virilizing 21-Hydroxylase Deficient Patient
S. Belli,
Melisa Taboas,
L. Dain,
2013,
Case reports in genetics.
S. Belli,
L. Dain,
T. Pasqualini,
2002,
Clinical endocrinology.
L. Dain,
J. Cotignola,
N. Buzzalino,
2019,
Molecular genetics & genomic medicine.
Javier Santos,
M. F. Pignataro,
L. Capece,
2021,
Archives of biochemistry and biophysics.