Hydrocephalus in an infant with trisomy 22.

Author:

Fahmi F,Schmerler S,Hutcheon R G

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Human chromosome 22;Kaplan, J.; Aurias, A.; Julier, C.; Prieur, M.; Szajnert, M.;J Med Genet,1987

2. The morbid anatomy of the human genome: chromosomal location of mutations causing disease;McKusick, V.A.; Amberger, J.S.;Med Genet,1993

3. A cytogenetic study of 1000 spontaneous abortions;Hassold, T.; Chen, N.; Funkhouser, J.;Ann Hum Genet,1980

4. Trisomy 22 in a 20 year old female;Welter, D.A.; L, III, Scharff; Teal, N.M.; Thevaos, T.G.;Hum Genet,1978

5. The ocular pathology of trisomy 22: report of two cases and review;Antle, C.M.; Pantzar, J.T.; White, V.A.;Pediatr Opthalmol Strabismus,1990

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1. Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case report;BMC Pediatrics;2023-03-18

2. Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report;Journal of Clinical Laboratory Analysis;2018-09-26

3. Syndromes associated with holoprosencephaly;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-05-17

4. Live-Born Trisomy 22: Patient Report and Review;Molecular Syndromology;2012

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