%0 Journal Article %1 Jong1991 %A Jong, G. De %A Fryns, J. P. %D 1991 %J Genet Couns %K , Newborn; African Continental Ancestry Group; Albinism, Oculocutaneous; Cerebral Palsy; Child, Preschool; Consanguinity; Diagnosis, Differential; Female; Hair Color; Humans; Infant; Mental Retardation; Microcephaly %N 3 %P 151--155 %T Oculocerebral syndrome with hypopigmentation (Cross syndrome): the mixed pattern of hair pigmentation as an important diagnostic sign. %V 2 %X The present report describes two female siblings of mixed ancestry (Cape Coloured) with consanguineous parents as further examples of Cross oculocerebral hypopigmentation syndrome. The mixed pattern of hair pigmentation as an important diagnostic sign is emphasized.

@article{Jong1991, abstract = {The present report describes two female siblings of mixed ancestry (Cape Coloured) with consanguineous parents as further examples of Cross oculocerebral hypopigmentation syndrome. The mixed pattern of hair pigmentation as an important diagnostic sign is emphasized.}, added-at = {2014-07-19T20:31:10.000+0200}, author = {Jong, G. De and Fryns, J. P.}, biburl = {https://www.bibsonomy.org/bibtex/2c6d98732d9e09df16143fc3e0b59d2a1/ar0berts}, groups = {public}, interhash = {cd11d2b14221479547c95fd476292cd3}, intrahash = {c6d98732d9e09df16143fc3e0b59d2a1}, journal = {Genet Couns}, keywords = {, Newborn; African Continental Ancestry Group; Albinism, Oculocutaneous; Cerebral Palsy; Child, Preschool; Consanguinity; Diagnosis, Differential; Female; Hair Color; Humans; Infant; Mental Retardation; Microcephaly}, number = 3, pages = {151--155}, pmid = {1801851}, timestamp = {2014-07-19T20:31:10.000+0200}, title = {Oculocerebral syndrome with hypopigmentation (Cross syndrome): the mixed pattern of hair pigmentation as an important diagnostic sign.}, username = {ar0berts}, volume = 2, year = 1991 }