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Silver staining of the supernumerary chromosome in the cat-eye syndrome.
Ann Genet. 1980;23(2):114-6.
Ann Genet. 1980.
PMID: 6156636
Partial trisomy 13 with phenotype of Patau syndrome due to maternal reciprocal translocation t(6;13) (q25;q13).
Ann Genet. 1980;23(1):57-9.
Ann Genet. 1980.
PMID: 6965845
No abstract available.
Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother.
Ann Genet. 1998;41(2):73-6.
Ann Genet. 1998.
PMID: 9706336
Interstital deletion of 13q associated with retinoblastoma and congenital malformations.
Ann Genet. 1979 Jun;22(2):106-7.
Ann Genet. 1979.
PMID: 315199
No abstract available.
XY/XXY mosaicism and fragile X syndrome.
Ann Genet. 1983;26(4):251-3.
Ann Genet. 1983.
PMID: 6607708
Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male.
Ann Genet. 1982;25(1):63-4.
Ann Genet. 1982.
PMID: 6979304
No abstract available.
Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome.
Am J Med Genet. 1992 Feb 1;42(3):343-5. doi: 10.1002/ajmg.1320420318.
Am J Med Genet. 1992.
PMID: 1536176
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