Results 121 to 130 of about 433 (176)
Approche moléculaire du syndrome humain de Waardenburg: clonage soustractif de gènes dérégulés dans le mutant murin correspondant SPLOTCH (Sp2H) [PDF]
, 1994 Van Helleputte, Françoise
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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida. [PDF]
J Med Genet, 1996 Hol FA +8 more
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Genetic analysis of autosomal recessive forms of retinitis pigmentosa [PDF]
, 1997 Bruford, Elspeth A.
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Genetic and phenotypic analysis of Danforth's short-tail mutation in the mouse [PDF]
, 1996 Alfred, Jane
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Functional conservation of the Drosophila gooseberry gene and its evolutionary alleles.
PLoS One, 2012 Liu W, Xue L.
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