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Cancer Detection and Prevention. Supplement : Official Publication of the International Society for Preventive Oncology, Inc|January 1, 1987
Immunocompetence in pregnancy: production of interleukin-2 by peripheral blood lymphocytesG J Hauser, A Lidor, V Zakuth, et al.
Human Mutation|January 1, 1994
Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 15, 2008
Rhombencephalosynapsis: prenatal imaging and autopsy findingsF McAuliffe, D Chitayat, W Halliday, et al.
American Journal of Medical Genetics|January 16, 1995
Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literatureD Chitayat, R H Ruvalcaba, R Babul, et al.
Human Biology|February 1, 1993
Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of QuebecC Dionne, C Gagné, P Julien, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
American Journal of Medical Genetics|March 1, 1990
Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?D Chitayat, B C McGillivray, R Rothstein, et al.
Genomics|June 21, 2001
Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutationsM Li, J Squire, C Shuman, et al.
American Journal of Medical Genetics|June 9, 1999
Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcomeD Chitayat, B Fernandez, A Gardner, et al.
American Journal of Medical Genetics|April 11, 2000
Inverted duplication of the distal short arm of chromosome 3 associated with lobar holoprosencephaly and lumbosacral meningomyeloceleD Kennedy, M M Silver, E J Winsor, et al.
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