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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 3
1955 3
1956 1
1957 1
1958 2
1960 2
1961 1
1962 1
1963 5
1964 2
1973 2
1978 3
1979 1
1981 1
1982 1
1990 1
1993 1
1996 1
1997 2
1999 1
2000 1
2001 1
2002 1
2003 1
2012 3
2013 3
2014 3
2015 4
2016 2
2017 3
2018 1
2019 3
2020 2
2021 2
2022 1
2023 1
2024 1
2025 0

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64 results

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Page 1
Congenital hypertrichosis universalis in Mexican female twins.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Valencia-Herrera A, Kofman S, Morán-Barroso V. Cervantes A, et al. Among authors: kofman s. Int J Dermatol. 2016 Jan;55(1):e29-31. doi: 10.1111/ijd.13104. Epub 2015 Oct 30. Int J Dermatol. 2016. PMID: 26518157 Review. No abstract available.
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Gómez-Laguna L, Martínez-Herrera A, Reyes-de la Rosa ADP, García-Delgado C, Nieto-Martínez K, Fernández-Ramírez F, Valderrama-Atayupanqui TY, Morales-Jiménez AB, Villa-Morales J, Kofman S, Cervantes A, Morán-Barroso VF. Gómez-Laguna L, et al. Among authors: kofman s. Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18. Ophthalmic Genet. 2018. PMID: 28922055 Review.
HYPERCALCEMIA OF MALIGNANCY.
BECKER FO, KOFMAN S. BECKER FO, et al. Among authors: kofman s. Presbyt St Lukes Hosp Med Bull. 1963 Oct;2:167-73. Presbyt St Lukes Hosp Med Bull. 1963. PMID: 14070025 Review. No abstract available.
64 results