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Year Number of Results
1963 1
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1967 2
1968 1
1969 3
1970 1
1972 1
1973 5
1974 3
1975 2
1977 1
1979 1
1980 1
1981 1
1982 3
1985 1
1988 1
1989 2
1990 4
1994 4
1995 2
1996 3
1997 1
1998 3
1999 3
2000 3
2002 1
2003 2
2004 2
2005 3
2006 1
2009 1
2011 1
2014 1
2016 1
2017 1
2024 0

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69 results

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Page 1
Old syndromes and new cytogenetics.
Punnett HH, Zakai EH. Punnett HH, et al. Dev Med Child Neurol. 1990 Sep;32(9):824-31. doi: 10.1111/j.1469-8749.1990.tb08489.x. Dev Med Child Neurol. 1990. PMID: 2227145 Review.
A case of cyclopia.
Batts JA Jr, Punnett HH, Valdes-Dapena M, Coles JW, Green WR. Batts JA Jr, et al. Among authors: punnett hh. Am J Obstet Gynecol. 1972 Mar;112(5):657-61. doi: 10.1016/0002-9378(72)90791-0. Am J Obstet Gynecol. 1972. PMID: 5059596
Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics.
Bieber FR, Cherry AM, Emanuel BS, Francke U, Hoyme HE, Jackson LG, Morton CC, Muenke M, Powell CM, Punnett HH, Rao PN, Schwartz S, Stevenson RE, Van Dyke DL. Bieber FR, et al. Among authors: punnett hh. Genet Med. 2017 Mar;19(3):294-296. doi: 10.1038/gim.2016.171. Epub 2016 Nov 17. Genet Med. 2017. PMID: 27854359 Free article.
Trisomy 22 mechanisms.
Punnett HH, Kistenmacher ML. Punnett HH, et al. Hum Genet. 1981;56(3):421. doi: 10.1007/BF00274706. Hum Genet. 1981. PMID: 7239526 No abstract available.
Definition of heterozygosity.
Punnett HH. Punnett HH. J Pediatr. 1982 Dec;101(6):1036. doi: 10.1016/s0022-3476(82)80041-3. J Pediatr. 1982. PMID: 7143159 No abstract available.
A report of three patients with an interstitial deletion of chromosome 15q24.
Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, Anderson CE, Punnett HH, Thurston VC, Sweeney D, Vance GH. Cushman LJ, et al. Among authors: punnett hh. Am J Med Genet A. 2005 Aug 15;137(1):65-71. doi: 10.1002/ajmg.a.30836. Am J Med Genet A. 2005. PMID: 16007617 Review.
DELETION OF SHORT ARM OF CHROMOSOME 5.
PUNNETT HH, CARPENTER GG, DIGEORGE AM. PUNNETT HH, et al. Lancet. 1964 Sep 12;2(7359):588. doi: 10.1016/s0140-6736(64)90656-7. Lancet. 1964. PMID: 14172376 No abstract available.
Clinical manifestations of familial 13;18 translocation.
Blattner WA, Kistenmacher ML, Tsai S, Punnett HH, Giblett ER. Blattner WA, et al. Among authors: punnett hh. J Med Genet. 1980 Oct;17(5):373-9. doi: 10.1136/jmg.17.5.373. J Med Genet. 1980. PMID: 7218277 Free PMC article.
5p14 deletion associated with microcephaly and seizures.
Johnson EI, Marinescu RC, Punnett HH, Tenenholz B, Overhauser J. Johnson EI, et al. Among authors: punnett hh. J Med Genet. 2000 Feb;37(2):125-7. doi: 10.1136/jmg.37.2.125. J Med Genet. 2000. PMID: 10662813 Free PMC article.
69 results