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1. CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY IN SWEDEN. I. EPIDEMIOLOGIC AND CLINICAL ASPECTS.

Authors: H O AKESSON
Journal: Acta Med Scand Date: 1964-01

2. Cutis verticis gyrata and chromosomal fragile sites.

Authors: S A Musumeci; R Ferri; M Viglianesi; M Elia; R M Ragusa; P Bergonzi
Journal: Am J Med Genet Date: 1991 Feb-Mar

3. Picture of the month. Cutis verticis gyrata.

Authors: I Felding; M Feingold
Journal: Am J Dis Child Date: 1988-03

4. In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence.

Authors: L J Russell; D D Weaver; M J Bull; M Weinbaum
Journal: Am J Med Genet Date: 1984-02

5. Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq.

Authors: M G Butler; G A Allen; J L Haynes; S J Clark
Journal: Am J Med Genet Date: 1990-10

6. Aetiological aspects of the cutis verticis gyrata and mental retardation syndrome.

Authors: J Palo; M Iivanainen; K Blomqvist; S Pesonen
Journal: J Ment Defic Res Date: 1970-03

7. Fetal brain disruption sequence.

Authors: C A Moore; D D Weaver; M J Bull
Journal: J Pediatr Date: 1990-03 Impact factor: 4.406

7 in total

1 in total

1. A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafness.

Authors: André Mégarbané; Rima Slim; Gudrun Nürnberg; Inga Ebermann; Peter Nürnberg; Hanno Jörn Bolz
Journal: Eur J Hum Genet Date: 2009-02-04 Impact factor: 4.246

1 in total