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Smigiel, R.
49
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Online (49)
Mediatypes
Articles (Online) (14)
OpenAccess-fulltext (35)
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1
DOZ047.94: The thoracoscopic approach for esophageal atresi..:
Patkowski, D
;
Gerus, S
;
Rasiewicz, M
...
Diseases of the Esophagus. 32 (2019) Supplement_1 - p. , 2019
Link:
https://doi.org/10.1093/..
?
2
DOZ047.58: The familial occurrence of congenital esophageal..:
Smigiel, R
;
Dzielendziak, A
;
Toczewski, K
...
Diseases of the Esophagus. 32 (2019) Supplement_1 - p. , 2019
Link:
https://doi.org/10.1093/..
?
3
DOZ047.23: How esophageal atresia affects the family life:
Rozensztrauch, A
;
Patkowski, D
;
Śmigiel, R
Diseases of the Esophagus. 32 (2019) Supplement_1 - p. , 2019
Link:
https://doi.org/10.1093/..
?
4
DOZ047.38: 10-years of experience with thoracoscopic approa..:
Dzielendziak, A
;
Toczewski, K
;
Śmigiel, R
.
Diseases of the Esophagus. 32 (2019) Supplement_1 - p. , 2019
Link:
https://doi.org/10.1093/..
?
5
New evidence for association of recessive IARS gene mutatio..:
Smigiel, R.
;
Biela, M.
;
Biernacka, A.
...
Clinical Genetics. 92 (2017) 6 - p. 671-673 , 2017
Link:
https://doi.org/10.1111/..
?
6
Is c.1431-12G>A A common European mutation of SPINK5? repor..:
Śmigiel, R
;
Królak-Olejnik, B
;
Śniegórska, D
...
Balkan Journal of Medical Genetics. 19 (2016) 2 - p. 81-84 , 2016
Link:
https://doi.org/10.1515/..
?
7
Alternations in genes expression of pathway signaling in es..:
Smigiel, R.
;
Lebioda, A.
;
Blaszczyński, M.
...
Diseases of the Esophagus. 28 (2014) 3 - p. 229-233 , 2014
Link:
https://doi.org/10.1111/..
?
8
Normal exon copy number of theGLI2andGLI3genes in patients ..:
Bednarczyk, D.
;
Smigiel, R.
;
Patkowski, D.
...
Diseases of the Esophagus. , 2013
Link:
https://doi.org/10.1111/..
?
9
Severe clinical course of Hirschsprung disease in a Mowat-W..:
Smigiel, R.
;
Szafranska, A.
;
Czyzewska, M.
...
Journal of Applied Genetics. 51 (2010) 1 - p. 111-113 , 2010
Link:
https://doi.org/10.1007/..
?
10
Use of Sliding-Window Fourier Transform in the Analysis of ..:
Smigiel, R.
;
Knoll, A.
;
Broll, N.
.
Materials Science Forum. 278-281 (1998) - p. 170-176 , 1998
Link:
https://doi.org/10.4028/..
?
11
Neurodevelopmental disorder in a patient with HMBS and SCN3..:
M, Kłaniewska
;
M, Rydzanicz
;
J, Bladowska
...
American Journal of Medical Genetics Part A. 194 (2024) 8 - p. , 2024
Link:
https://doi.org/10.1002/..
?
12
Metabolic Parameters in Patients with Prader-Willi Syndrome..:
Krefft M
;
Frydecka D
;
Śmigiel R
.
https://www.dovepress.com/metabolic-parameters-in-patients-with-prader-willi-syndrome-and-digeor-peer-reviewed-article-NDT. , 2020
Link:
https://doaj.org/article..
?
13
Mowat-Wilson syndrome : growth charts:
Ivanovski I
;
Djuric O
;
Broccoli S
...
info:eu-repo/semantics/altIdentifier/pmid/32539836. , 2020
Link:
http://hdl.handle.net/24..
?
14
Mowat-Wilson syndrome: growth charts:
Ivanovski I
;
Djuric O
;
Broccoli S
...
info:eu-repo/semantics/altIdentifier/pmid/32539836. , 2020
Link:
http://hdl.handle.net/11..
?
15
Mowat-Wilson syndrome: Growth charts:
Ivanovski I
;
Djuric O
;
Broccoli S
...
info:eu-repo/semantics/altIdentifier/pmid/32539836. , 2020
Link:
http://hdl.handle.net/11..
1-15