An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly

No abstract is available for this paper.

• Publication year

  1977

• Venue

  Clinical Genetics

• Publication date

  1977-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/j.1399-0004.1977.tb00903.xPMID 891015
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Familial holoprosencephaly.

  1971cited by this paper
• Familial Holoprosencephaly

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• Familial predisposition in man.

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• The inheritance of liability to certain diseases, estimated from the incidence among relatives

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• The simulation of mendelism.

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• Dominantly inherited microcephaly, short stature and normal intelligence.

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• Brains and faces in holoprosencephaly: pre‐ and postnatal description of 30 cases

  2002cites this paper
• A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36

  1995cites this paper
• Fetal cleft lip and palate: sonographic diagnosis and postnatal outcome.

  1993cites this paper
• Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies.

  1992cites this paper
• Dominantly inherited microcephaly, short stature and normal intelligence

  1992cites this paper
• Five cases of DeMyer sequence: an interophthalmic dysplasia.

  1991cites this paper
• A catalogue of multiple congenital anomaly syndromes

  1991cites this paper
• Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.

  1989cites this paper
• Holoprosencephaly: a developmental field defect.

  1989cites this paper
• Autosomal dominant inheritance of the DeMyer Sequence.

  1988cites this paper
• Microcephaly in familial holoprosencephaly.

  1988cites this paper
• Median cleft of the upper lip associated with lipomas of the central nervous system and cutaneous polyps.

  1987cites this paper
• Orbital hypotelorism. An isolated autosomal dominant trait.

  1984cites this paper
• Familial agnathia-holoprosencephaly.

  1983cites this paper
• Recurrence of holoprosencephaly in families with a positive history.

  1983cites this paper
• An update on the holoprosencephalic disorders.

  1982cites this paper
• Holoprosencephaly is an etiologically heterogeneous condition. Recently a number of new causes have come to light, several syndromes have been delineated or partially delineated, and a few associations have become apparent. This article updates the nosology of human holoprosencephaly.

  1982cites this paper
• Holoprosencephaly. Computerized tomographic and pneumographic findings with anatomic correlation.

  1980cites this paper
• Reply to Escobar and Cantu

  1979cites this paper