Phadke S - Search Results

1

First International Conference on RASopathies and Neurofibromatoses in Asia: Identification and advances of new therapeutics.

Rauen KA, Alsaegh A, Ben-Shachar S, Berman Y, Blakeley J, Cordeiro I, Elgersma Y, Evans DG, Fisher MJ, Frayling IM, George J, Huson SM, Kerr B, Khire U, Korf B, Legius E, Messiaen L, van Minkelen R, Nampoothiri S, Ngeow J, Parada LF, Phadke S, Pillai A, Plotkin SR, Puri R, Raji A, Ramesh V, Ratner N, Shankar SP, Sharda S, Tambe A, Vikkula M, Widemann BC, Wolkenstein P, Upadhyaya M. Rauen KA, et al. Among authors: phadke s. Am J Med Genet A. 2019 Jun;179(6):1091-1097. doi: 10.1002/ajmg.a.61125. Epub 2019 Mar 25. Am J Med Genet A. 2019. PMID: 30908877 Free PMC article.

2

Further delineation of mandibulofacial dysostosis: Toriello type.

Puri RD, Phadke SR. Puri RD, et al. Clin Dysmorphol. 2002 Apr;11(2):91-3. doi: 10.1097/00019605-200204000-00003. Clin Dysmorphol. 2002. PMID: 12002155

3

Recurrence of complex camptopolydactyly in a sibling suggestive of autosomal recessive mode of inheritance.

Phadke SR, Agarwal S, Puri RD. Phadke SR, et al. Am J Med Genet A. 2003 Jan 1;116A(1):94-6. doi: 10.1002/ajmg.a.10086. Am J Med Genet A. 2003. PMID: 12476460 No abstract available.

4

Catel-Manzke syndrome without cleft palate: a case report.

Puri RD, Phadke SR. Puri RD, et al. Clin Dysmorphol. 2003 Oct;12(4):279-81. doi: 10.1097/00019605-200310000-00015. Clin Dysmorphol. 2003. PMID: 14564220

5

Genetic counseling: the impact in Indian milieu.

Phadke SR, Pandey A, Puri RD, Patil SJ. Phadke SR, et al. Indian J Pediatr. 2004 Dec;71(12):1079-82. doi: 10.1007/BF02829818. Indian J Pediatr. 2004. PMID: 15630315

6

Hemihyperplasia syndromes.

Dalal AB, Phadke SR, Pradhan M, Sharda S. Dalal AB, et al. Among authors: phadke sr. Indian J Pediatr. 2006 Jul;73(7):609-15. doi: 10.1007/BF02759927. Indian J Pediatr. 2006. PMID: 16877856

7

Issues in counseling for Down syndrome.

Girisha KM, Sharda SV, Phadke SR. Girisha KM, et al. Indian Pediatr. 2007 Feb;44(2):131-3. Indian Pediatr. 2007. PMID: 17351304 Free article.

8

Uptake of invasive prenatal diagnostic tests in women after detection of soft markers for chromosomal abnormality on ultrasonographic evaluation.

Sharda S, Phadke SR. Sharda S, et al. Among authors: phadke sr. J Perinatol. 2007 Sep;27(9):550-5. doi: 10.1038/sj.jp.7211787. Epub 2007 Jul 5. J Perinatol. 2007. PMID: 17611609

9

A report of a patient with interstitial deletion of 15q22: further delineation of a new micro deletion syndrome.

Phadke SR, Sharda S. Phadke SR, et al. Am J Med Genet A. 2008 Aug 1;146A(15):1999-2000. doi: 10.1002/ajmg.a.32043. Am J Med Genet A. 2008. PMID: 18627036 No abstract available.

10

Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from India.

Phadke SR, Gupta N, Girisha KM, Kabra M, Maeda M, Vidal E, Moser A, Steinberg S, Puri RD, Verma IC, Braverman N. Phadke SR, et al. J Appl Genet. 2010;51(1):107-10. doi: 10.1007/BF03195717. J Appl Genet. 2010. PMID: 20145307

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

469 results

Search Page

Filters