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Fingerprint Dive into the research topics where Surasak Puvabanditsin is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Newborn Infant Medicine & Life Sciences
Chromosome Deletion Medicine & Life Sciences
Trisomy Medicine & Life Sciences
Monosomy Medicine & Life Sciences
Fatal Outcome Medicine & Life Sciences
Imperforate Anus Medicine & Life Sciences
Umbilical Cord Medicine & Life Sciences
Dandy-Walker Syndrome Medicine & Life Sciences

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Research Output 1995 2019

  • 256 Citations
  • 9 h-Index
  • 46 Article
  • 3 Letter
  • 2 Review article
  • 1 Comment/debate

8p11 Microduplication Is Associated with Neonatal Stridor

Puvabanditsin, S., Gengel, N., Botti, C., Jacob, M., Jalil, M., Cabrera, K. & Mehta, R., Jan 1 2019, In : Molecular Syndromology. 9, 6, p. 324-327 4 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 8
Aortic Coarctation
Respiratory Sounds
Microarray Analysis
1 Citation (Scopus)

Cleidocranial dysplasia with 6p21.1-p12.3 microdeletion: A case report and literature review

Puvabanditsin, S., February, M., Mayne, J., McConnell, J. & Meht, R., Jan 1 2018, In : Cleft Palate-Craniofacial Journal. 55, 6, p. 891-894 4 p.

Research output: Contribution to journalArticle

Cleidocranial Dysplasia
Inheritance Patterns
Inborn Genetic Diseases

Congenital second-degree heart block and total anomalous pulmonary venous return associated with microduplication of 1q32.2

Puvabanditsin, S., Puthenpura, V., Gueye-Ndiaye, S., Takyi, M., Madubuko, A., Walzer, L. & Mehta, R., May 1 2018, In : Annals of Pediatric Cardiology. 11, 2, p. 194-196 3 p.

Research output: Contribution to journalArticle

Scimitar Syndrome
Heart Block
Chromosome Duplication
Microarray Analysis
Oligonucleotide Array Sequence Analysis

Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region

Puvabanditsin, S., Chen, C. W., Botwinick, M., Hussein, K., Mariduena, J. & Mehta, R., Jul 1 2018, In : Clinical Case Reports. 6, 7, p. 1268-1275 8 p.

Research output: Contribution to journalArticle

Jacobsen Distal 11q Deletion Syndrome
Newborn Infant
Chromosomes, Human, Pair 11
1 Citation (Scopus)

Bile-stained amniotic fluid: A case report

Puvabanditsin, S., Chen, C. W., Vinod, S., Mehta, M. S., Choudry, O. & Walzer, L., Sep 6 2017, In : Journal of Medical Case Reports. 11, 1, 254.

Research output: Contribution to journalArticle

Amniotic Fluid
Intestinal Atresia