Chitayat D - Search Results

1

An Additional Individual with a De Novo Variant in Myelin Regulatory Factor (MYRF) with Cardiac and Urogenital Anomalies: Further Proof of Causality: Comments on the article by Pinz et al. ().

Chitayat D, Shannon P, Uster T, Nezarati MM, Schnur RE, Bhoj EJ. Chitayat D, et al. Am J Med Genet A. 2018 Sep;176(9):2041-2043. doi: 10.1002/ajmg.a.40360. Epub 2018 Aug 2. Am J Med Genet A. 2018. PMID: 30070761 No abstract available.

2

King syndrome: a genetically heterogenous phenotype due to congenital myopathies.

Chitayat D, Hodgkinson KA, Ginsburg O, Dimmick J, Watters GV. Chitayat D, et al. Am J Med Genet. 1992 Aug 1;43(6):954-6. doi: 10.1002/ajmg.1320430610. Am J Med Genet. 1992. PMID: 1415346 Review.

3

Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndrome.

Chitayat D, Hodgkinson KA, Chen MF, Haber GD, Nakishima S, Sando I. Chitayat D, et al. Am J Med Genet. 1992 Aug 1;43(6):970-5. doi: 10.1002/ajmg.1320430613. Am J Med Genet. 1992. PMID: 1415348

4

Acrania: a manifestation of the Adams-Oliver syndrome.

Chitayat D, Meunier C, Hodgkinson KA, Robb L, Azouz M. Chitayat D, et al. Am J Med Genet. 1992 Nov 15;44(5):562-6. doi: 10.1002/ajmg.1320440506. Am J Med Genet. 1992. PMID: 1481809

5

Familial intestinal malrotation with midgut volvulus and facial anomalies: a disorder involving a gene controlling the normal gut rotation?

Stalker HJ, Chitayat D. Stalker HJ, et al. Among authors: chitayat d. Am J Med Genet. 1992 Sep 1;44(1):46-7. doi: 10.1002/ajmg.1320440111. Am J Med Genet. 1992. PMID: 1519649

6

Robin sequence with facial and digital anomalies in two half-brothers by the same mother.

Chitayat D, Meunier CM, Hodgkinson KA, Azouz ME. Chitayat D, et al. Am J Med Genet. 1991 Aug 1;40(2):167-72. doi: 10.1002/ajmg.1320400209. Am J Med Genet. 1991. PMID: 1897570

7

Syndrome of mental retardation and distal arthrogryposis in sibs.

Chitayat D, Hodgkinson KA, Blaichman S, Chen ME, Watters GV, Khalife S, Hall JG. Chitayat D, et al. Am J Med Genet. 1991 Oct 1;41(1):49-51. doi: 10.1002/ajmg.1320410114. Am J Med Genet. 1991. PMID: 1951463

8

Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.

Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ. Chitayat D, et al. Am J Med Genet. 1990 Sep;37(1):65-70. doi: 10.1002/ajmg.1320370116. Am J Med Genet. 1990. PMID: 2240046

9

Congenital heart disease and Robinow syndrome: coincidence or an additional component of the syndrome?

Webber SA, Wargowski DS, Chitayat D, Sandor GG. Webber SA, et al. Among authors: chitayat d. Am J Med Genet. 1990 Dec;37(4):519-21. doi: 10.1002/ajmg.1320370418. Am J Med Genet. 1990. PMID: 2260599 Review.

10

Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?

Chitayat D, McGillivray BC, Rothstein R, Flodmark O, Priddy RW, Ebelt VJ, Lirenman DS, Hall JG. Chitayat D, et al. Am J Med Genet. 1990 Mar;35(3):406-14. doi: 10.1002/ajmg.1320350318. Am J Med Genet. 1990. PMID: 2309790

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