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Author/Creator Ambrozaitytė, Laima

2. Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. Issue 1 (December 2016)

Authors:
Sachwitz, Jana; Strobl-Wildemann, Getrud; Fekete, György; Ambrozaitytė, Laima; Kučinskas, Vaidutis; Soellner, Lukas; Begemann, Matthias; Eggermann, Thomas
Journal:
BMC medical genetics
Issue:
Volume 17:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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3. Frame shift mutations of the ZMPSTE24 gene in two siblings with restrictive dermopathy. Issue 1 (January 2016)

Authors:
Matulevičienė, Aušra; Meškienė, Raimonda; Morkūnienė, Aušra; Ambrozaitytė, Laima; Meškauskas, Raimundas; Garunkštienė, Rasa; Drazdienė, Nijolė; Utkus, Algirdas; Kučinskas, Vaidutis
Journal:
Clinical dysmorphology
Issue:
Volume 25:Issue 1(2016:Jan.)
Page Start:
Record Type:
Journal Article
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5. Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: A case report. Issue 16 (April 2017)

Authors:
Aleksiūnienė, Beata; Matulevičiūtė, Rugilė; Matulevičienė, Aušra; Burnytė, Birutė; Krasovskaja, Natalija; Ambrozaitytė, Laima; Mikštienė, Violeta; Dirsė, Vaidas; Utkus, Algirdas; Kučinskas, Vaidutis
Other Names:
Zhu. Xiaolin section editor.
Journal:
Medicine
Issue:
Volume 96:Issue 16(2017)
Page Start:
Record Type:
Journal Article
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6. Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families. Issue 3 (12th December 2019)

Authors:
Preiksaitiene, Egle; Voisin, Norine; Gueneau, Lucie; Benušienė, Eglė; Krasovskaja, Natalija; Blažytė, Evelina Marija; Ambrozaitytė, Laima; Rančelis, Tautvydas; Reymond, Alexandre; Kučinskas, Vaidutis
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 3(2020)
Page Start:
536
Record Type:
Journal Article
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