Normal view MARC view ISBD view

[Polyps of the ear]. [electronic resource]

By:

CASTILLO MORALES, A J

Producer: 20030501Description: 405-40 p. digitalISSN:

0001-6500

Subject(s):

In: Acta oto-rino-laringologica ibero-americana vol. 4

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article

There are no comments on this title.

to post a comment.

Back to results

881 Chromosome 6p25 deletion syndrome: report of a case with optic disc coloboma and review of published ophthalmic findings.
by Beby, Francis
882 Neuropsychological and behavioural phenotype of Dandy-Walker variant presenting in chromosome 22 trisomy: a case study.
by Searson, Ruth
883 Revised classification of posterior fossa cysts and cystlike malformations based on the results of multiplanar MR imaging.
by Barkovich, A J
884 Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.
by Schuster, V
885 Increased nuchal translucency thickness: a potential indicator for Ritscher-Schinzel syndrome.
by Rusnak, Alison J
886 Familial occurrence of isolated Dandy-Walker variant in two consecutive male fetuses.
by Lin, Y H
887 Discrepancy in fetal sex assignment between cell free fetal DNA and ultrasound.
by Iruretagoyena, J I
888 Prenatal diagnosis of trisomy 9 mosaic presenting as a case of Dandy-Walker malformation.
by Bureau, Y A
889 Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation.
by Metzke-Heidemann, S
890 Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions.
by Ferraris, Alessandro
891 Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia.
by Zou, Zhiyong
892 Posterior fossa abnormalities in children with infantile spasms.
by Schiffmann, R
893 Cystic retrocerebellar malformations: unification of the Dandy-Walker complex and the Blake's pouch cyst.
by Strand, R D
894 De novo pure 12q22q24.33 duplication: first report of a case with mental retardation, ADHD, and Dandy-Walker malformation.
by Cappellacci, S
895 A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.
by Chen, Chih-Ping
896 Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis.
by Blank, Marissa C
897 Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34.
by Mimaki, Masakazu
898 Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.
by Schoner, Katharina
899 The "keyhole": a sign of herniation of a trapped fourth ventricle and other posterior fossa cysts.
by Wolfson, B J
900 Description of the smallest critical region for Dandy-Walker malformation in chromosome 13 in a girl with a cryptic deletion related to t(6;13)(q23;q32).
by Mademont-Soler, Irene