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Mulatinho, Milene
15
results:
Search for persons
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Format
Online (15)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (6)
Sorted by: Relevance
Sorted by: Year
?
1
Maternal Uniparental Disomy 14 (UPD14) Identified by Clinic..:
Chan, Alvin P.
;
Mulatinho, Milene
;
Iskander, Paul
...
ACG Case Reports Journal. 6 (2019) 3 - p. e00021 , 2019
Link:
https://doi.org/10.14309..
?
2
53. Multidimensional cytogenetics workup on a rare chromoso..:
Mulatinho, Milene
;
Kantarci, Sibel
;
Crandall, Barbara
..
Cancer Genetics. 224-225 (2018) - p. 70 , 2018
Link:
https://doi.org/10.1016/..
?
3
Microdeletion of ZBTB20 Results in a Phenotype Overlapping ..:
Mulatinho, Milene
;
Tenney, Jessica
;
Vilain, Eric
.
Cancer Genetics. 209 (2016) 5 - p. 244-245 , 2016
Link:
https://doi.org/10.1016/..
?
4
Microdeletion and Microduplication Syndromes:
Weise, Anja
;
Mrasek, Kristin
;
Klein, Elisabeth
...
Journal of Histochemistry & Cytochemistry. 60 (2012) 5 - p. 346-358 , 2012
Link:
https://doi.org/10.1369/..
?
5
Deletion (1)(p32.2–p32.3) detected by array‐CGH in a patien..:
Mulatinho, Milene
;
Llerena, Juan
;
Leren, Trond P.
..
American Journal of Medical Genetics Part A. 146A (2008) 17 - p. 2284-2290 , 2008
Link:
https://doi.org/10.1002/..
?
6
De novo loss‐of‐function variants in STAG2 are associated w..:
Mullegama, Sureni V.
;
Klein, Steven D.
;
Mulatinho, Milene V.
...
American Journal of Medical Genetics Part A. 173 (2017) 5 - p. 1319-1327 , 2017
Link:
https://doi.org/10.1002/..
?
7
Severe intellectual disability, omphalocele, hypospadia and..:
Mulatinho, Milene Vianna
;
de Carvalho Serao, Cassio Luiz
;
Scalco, Fernanda
...
Molecular Cytogenetics. 5 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
?
8
A New Multicolor Fluorescence In Situ Hybridization Probe S..:
Bucksch, Maria
;
Ziegler, Monika
;
Kosayakova, Nadezda
...
Journal of Histochemistry & Cytochemistry. 60 (2012) 7 - p. 530-536 , 2012
Link:
https://doi.org/10.1369/..
?
9
Cytogenetic and molecular studies of an X;21 translocation ..:
Cardoso, Leila C.A.
;
Moraes, Lúcia
;
Camilo, Maria Jesus E.
...
European Journal of Medical Genetics. 51 (2008) 6 - p. 588-597 , 2008
Link:
https://doi.org/10.1016/..
?
10
Maternal Uniparental Disomy 14 (UPD14) Identified by Clinic..:
Chan, Alvin P
;
Mulatinho, Milene
;
Iskander, Paul
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658016/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
11
Microdeletion and Microduplication Syndromes:
Weise, Anja
;
Mrasek, Kristin
;
Klein, Elisabeth
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351230. , 2012
Link:
http://www.ncbi.nlm.nih...
?
12
Severe intellectual disability, omphalocele, hypospadia and..:
Mulatinho, Milene
;
de Carvalho Serao, Cassio
;
Scalco, Fernanda
...
qt00n2q9wn. , 2012
Link:
https://escholarship.org..
?
13
Severe intellectual disability, omphalocele, hypospadia and..:
Mulatinho Milene
;
de Carvalho Serao Cassio
;
Scalco Fernanda
...
http://www.molecularcytogenetics.org/content/5/1/30. , 2012
Link:
https://doi.org/10.1186/..
?
14
Severe intellectual disability, omphalocele, hypospadia and..:
Mulatinho, Milene
;
de Carvalho Serao, Cassio
;
Scalco, Fernanda
...
http://www.molecularcytogenetics.org/content/5/1/30. , 2012
Link:
http://www.molecularcyto..
?
15
A New Multicolor Fluorescence In Situ Hybridization Probe S..:
Bucksch, Maria
;
Ziegler, Monika
;
Kosayakova, Nadezda
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460354. , 2012
Link:
http://www.ncbi.nlm.nih...
1-15
