Chitayat D - Search Results

1

Lethal congenital muscular dystrophy with cataracts and a minor brain anomaly: new entity or variant of Walker-Warburg syndrome?

Wargowski DS, Chitayat D, Tyson RW, Norman MG, Friedman JM. Wargowski DS, et al. Among authors: chitayat d. Am J Med Genet. 1991 Apr 1;39(1):19-24. doi: 10.1002/ajmg.1320390106. Am J Med Genet. 1991. PMID: 1867258

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

Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study.

Wilson RD, Chitayat D, McGillivray BC. Wilson RD, et al. Among authors: chitayat d. Am J Med Genet. 1992 Nov 15;44(5):586-90. doi: 10.1002/ajmg.1320440511. Am J Med Genet. 1992. PMID: 1481814

4

Skeletal dysplasia, intracerebral calcifications, optic atrophy, hearing impairment, and mental retardation: nosology of dysosteosclerosis.

Chitayat D, Silver K, Azouz EM. Chitayat D, et al. Am J Med Genet. 1992 Jun 1;43(3):517-23. doi: 10.1002/ajmg.1320430304. Am J Med Genet. 1992. PMID: 1605243

5

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

6

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.

7

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

8

Hypomelanosis of Ito--a nonspecific marker of somatic mosaicism: report of case with trisomy 18 mosaicism.

Chitayat D, Friedman JM, Johnston MM. Chitayat D, et al. Am J Med Genet. 1990 Mar;35(3):422-4. doi: 10.1002/ajmg.1320350320. Am J Med Genet. 1990. PMID: 2309792

9

Neuroblastoma in a child with Wiedemann-Beckwith syndrome.

Chitayat D, Friedman JM, Dimmick JE. Chitayat D, et al. Am J Med Genet. 1990 Mar;35(3):433-6. doi: 10.1002/ajmg.1320350322. Am J Med Genet. 1990. PMID: 2309794

10

Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndrome.

Chitayat D, Rothchild A, Ling E, Friedman JM, Couch RM, Yong SL, Baldwin VJ, Hall JG. Chitayat D, et al. Am J Med Genet. 1990 Aug;36(4):434-9. doi: 10.1002/ajmg.1320360412. Am J Med Genet. 1990. PMID: 2389800

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