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1. Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly.

Authors: I D Young; D J Madders
Journal: J Med Genet Date: 1987-11 Impact factor: 6.318

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Review 1. Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literature.

Authors: Sophia M Bous; Benjamin D Solomon; Luitgard Graul-Neumann; Heidemarie Neitzel; Emily E Hardisty; Maximilian Muenke
Journal: Clin Dysmorphol Date: 2012-10 Impact factor: 0.816

2. Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome.

Authors: H Bachman; R D Clark; W Salahi
Journal: J Med Genet Date: 1990-01 Impact factor: 6.318

3. A single morphogenetic field gives rise to two retina primordia under the influence of the prechordal plate.

Authors: H Li; C Tierney; L Wen; J Y Wu; Y Rao
Journal: Development Date: 1997-02 Impact factor: 6.868

Review 4. Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Authors: A Verloes; S Aymé; D Gambarelli; M Gonzales; M Le Merrer; N Mulliez; N Philip; J Roume
Journal: J Med Genet Date: 1991-05 Impact factor: 6.318

4 in total