Pitfalls of genetic counselling in Pfeiffer's syndrome.

Author:

Baraitser M,Bowen-Bravery M,Saldana-Garcia P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference8 articles.

1. Mendelian inheritance in man;McKusick, V.A.,1978

2. Recognizable patterns of human malformation. Major problems in clinical pediatrics;Smith, D.W.,1976

3. Acrocephalopolysyndactyly, type Noack, in a large kindred;Robinow, M.; Sorauf, T.J.;Birth Defects,1975

4. Craniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindred;Jackson, C.E.; Weiss, L.; Reynolds, W.A.; Forman, T.F.; Petersen, J.A.;J Pediatr,1976

5. The acrocephalosyndactyly syndrome: a metacarpophalangeal pattern profile analysis;Escobar, V.; Bixler, D.;Clin Genet,1977

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2. Genetic Causes of Craniosynostosis: An Update;Molecular Syndromology;2018-08-15

3. Pfeiffer Syndrome;Journal of Craniofacial Surgery;2013-01

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