Malik S - Search Results

1

Complex postaxial polydactyly types A and B with camptodactyly, hypoplastic third toe, zygodactyly and other digit anomalies caused by a novel GLI3 mutation.

Mumtaz S, Yıldız E, Lal K, Tolun A, Malik S. Mumtaz S, et al. Among authors: malik s. Eur J Med Genet. 2017 May;60(5):268-274. doi: 10.1016/j.ejmg.2017.03.004. Epub 2017 Mar 14. Eur J Med Genet. 2017. PMID: 28315472

2

Autosomal dominant syndrome of camptodactyly, clinodactyly, syndactyly, and bifid toes.

Malik S, Afzal M, Gul S, Wahab A, Ahmad M. Malik S, et al. Am J Med Genet A. 2010 Sep;152A(9):2313-7. doi: 10.1002/ajmg.a.33552. Am J Med Genet A. 2010. PMID: 20683984

3

Zygodactyly with thumb aplasia: an unusual variant in a male subject.

Malik S, Jabeen N. Malik S, et al. J Coll Physicians Surg Pak. 2011 Nov;21(11):710-2. J Coll Physicians Surg Pak. 2011. PMID: 22078357

4

Clinical and descriptive genetic study of polydactyly: a Pakistani experience of 313 cases.

Malik S, Ullah S, Afzal M, Lal K, Haque S. Malik S, et al. Clin Genet. 2014 May;85(5):482-6. doi: 10.1111/cge.12217. Epub 2013 Jul 5. Clin Genet. 2014. PMID: 23772746

5

Polydactyly: phenotypes, genetics and classification.

Malik S. Malik S. Clin Genet. 2014 Mar;85(3):203-12. doi: 10.1111/cge.12276. Epub 2013 Oct 18. Clin Genet. 2014. PMID: 24020795 Review.

6

Study of non-syndromic thumb aplasia in six independent cases.

Riaz HF, Lal K, Ahmad B, Shuaib M, Naqvi SF, Malik S. Riaz HF, et al. Among authors: malik s. Pak J Med Sci. 2014 May;30(3):677-81. doi: 10.12669/pjms.303.4626. Pak J Med Sci. 2014. PMID: 24949004 Free PMC article.

7

Mutations affecting the BHLHA9 DNA-binding domain cause MSSD, mesoaxial synostotic syndactyly with phalangeal reduction, Malik-Percin type.

Malik S, Percin FE, Bornholdt D, Albrecht B, Percesepe A, Koch MC, Landi A, Fritz B, Khan R, Mumtaz S, Akarsu NA, Grzeschik KH. Malik S, et al. Am J Hum Genet. 2014 Dec 4;95(6):649-59. doi: 10.1016/j.ajhg.2014.10.012. Epub 2014 Nov 13. Am J Hum Genet. 2014. PMID: 25466284 Free PMC article.

8

Congenital hypoplasia of first digital ray of hands as an isolated presentation in four subjects.

Lal K, Mumtaz S, Rehman AU, Bibi M, Pervin Z, Malik S. Lal K, et al. Among authors: malik s. Pak J Med Sci. 2014 Nov-Dec;30(6):1428-31. doi: 10.12669/pjms.306.5464. Pak J Med Sci. 2014. PMID: 25674153 Free PMC article.

9

Congenital constriction ring of limbs in subjects with history of maternal substance use.

Malik S, Lal K, Fatima NG, Samo A, Haque S. Malik S, et al. J Coll Physicians Surg Pak. 2015 May;25(5):383-5. J Coll Physicians Surg Pak. 2015. PMID: 26008671

10

RBBP8 syndrome with microcephaly, intellectual disability, short stature and brachydactyly.

Mumtaz S, Yıldız E, Jabeen S, Khan A, Tolun A, Malik S. Mumtaz S, et al. Among authors: malik s. Am J Med Genet A. 2015 Dec;167A(12):3148-52. doi: 10.1002/ajmg.a.37299. Epub 2015 Sep 3. Am J Med Genet A. 2015. PMID: 26333564

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