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1
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Decreasing late mortality among five-year survivors of cancer in childhood and adolescence: a population-based study in the Nordic countries.
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J Clin Oncol
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2001
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2.48
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2
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Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide.
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J Med Genet
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2003
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2.03
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3
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Pallister-Killian syndrome: cytogenetic and molecular studies.
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Clin Genet
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1987
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1.13
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4
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Congenital malformations in twins: an international study.
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Am J Med Genet
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1999
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1.10
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5
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Cancer in siblings of children with cancer in the Nordic countries: a population-based cohort study.
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Lancet
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2001
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1.01
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6
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Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems.
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Am J Med Genet
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2000
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1.00
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7
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Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood sample.
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Prenat Diagn
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1989
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0.88
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8
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Major congenital anomalies in children born after frozen embryo transfer: a cohort study 1995-2006.
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Hum Reprod
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2014
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0.85
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9
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Craniofrontonasal dysostosis: variable expression in a three-generation family.
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Clin Genet
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1990
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0.85
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10
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Molecular cytogenetic study of patients with Pallister-Killian syndrome.
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Hum Genet
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1993
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0.84
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11
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Cardio-facio-cutaneous syndrome: three additional cases and review of the literature.
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Am J Med Genet
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1992
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0.81
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12
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On the symmetry of limb deficiencies among children with multiple congenital anomalies.
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Ann Genet
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2001
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0.81
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13
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Congenital anomalies and first life year surveillance in Type 1 diabetic births.
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Diabet Med
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2002
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0.75
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