Chitayat D - Search Results

1

Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy.

Lehman AM, Eydoux P, Doherty D, Glass IA, Chitayat D, Chung BY, Langlois S, Yong SL, Lowry RB, Hildebrandt F, Trnka P. Lehman AM, et al. Among authors: chitayat d. Am J Med Genet A. 2010 Jun;152A(6):1411-9. doi: 10.1002/ajmg.a.33416. Am J Med Genet A. 2010. PMID: 20503315 Free PMC article.

2

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

3

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

4

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

5

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

6

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

7

De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.

Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG. Chitayat D, et al. Am J Med Genet. 1989 Jan;32(1):36-41. doi: 10.1002/ajmg.1320320109. Am J Med Genet. 1989. PMID: 2495721

8

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG. Bamforth JS, et al. Among authors: chitayat d. Am J Med Genet. 1989 Jan;32(1):93-9. doi: 10.1002/ajmg.1320320120. Am J Med Genet. 1989. PMID: 2650550

9

Hepatocellular carcinoma in a child with familial Russell-Silver syndrome.

Chitayat D, Friedman JM, Anderson L, Dimmick JE. Chitayat D, et al. Am J Med Genet. 1988 Dec;31(4):909-14. doi: 10.1002/ajmg.1320310425. Am J Med Genet. 1988. PMID: 2853572

10

Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis.

Chitayat D, McGillivray BC, Wood S, Kalousek DK, Langlois S, Applegarth DA. Chitayat D, et al. Am J Med Genet. 1988 Nov;31(3):655-61. doi: 10.1002/ajmg.1320310321. Am J Med Genet. 1988. PMID: 3228144

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