Autosomal dominant inheritance of the DeMyer Sequence.

No abstract is available for this paper.

• Publication year

  1988

• Venue

  Journal of Craniofacial Genetics and Developmental Biology

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  PMID 3209682
• 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.

• Diagnosis and Management of Fetal Holoprosencephaly

  1985cited by this paper
• Prenatal diagnosis of semilobar holoprosencephaly.

  1984cited by this paper
• What is the incidence of holoprosencephaly?

  1984cited by this paper
• The obstetric significance of holoprosencephaly.

  1984cited by this paper
• Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.

  1984cited by this paper
• Single central incisor in familial holoprosencephaly.

  1984cited by this paper
• Holoprosencephaly in infants of diabetic mothers.

  1983cited by this paper
• Antenatal ultrasound diagnosis of holoprosencephaly: a case report.

  1982cited by this paper
• Median cerebrofacial dysgenesis: the syndrome of median facial defects with hypotelorism.

  1978cited by this paper
• An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly

  1977cited by this paper
• Letter: Holoprosencephaly.

  1974cited by this paper
• Genetic Heterogeneity of Cebocephaly

  1974cited by this paper
• Holoprosencephaly with median cleft lip. Clinical, pathological, and echoencephalographic study.

  1972cited by this paper
• [The cyclops. Clinical and anatomical study of a familial cyclopia].

  1971cited by this paper
• Familial Holoprosencephaly

  1970cited by this paper
• Familial holoprosencephaly with endocrine dysgenesis.

  1968cited by this paper
• Cyclopism as a Hereditary Malformation

  1968cited by this paper
• Hereditary brachial and cranial neuritis genetically linked with ocular hypotelorism and syndactyly.

  1968cited by this paper
• THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY).

  1964cited by this paper
• Familial alobar holoprosencephaly (arhinencephaly) with median cleft lip and palate

  1963cited by this paper
• [Olfacto-genital dysplasia (agenesis of the olfactory lobes with absence of gonadal development at puberty].

  1960cited by this paper

• Solitary maxillary central incisor and short stature. Craniofacial analysis of a patient

  2017cites this paper
• Universidade de São Paulo Hospital de Reabilitação de Anomalias Craniofaciais Holoprosencefalia: Clínica e Linguagem

  2006cites this paper
• Solitary median maxillary central incisor syndrome: Clinical case with a novel mutation of sonic hedgehog

  2004cites this paper
• SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.

  2001cites this paper
• Solitary median maxillary central incisor, short stature, choanal atresia/midnasal stenosis (SMMCI) syndrome.

  1997cites this paper
• Holoprosencephaly: a family showing dominant inheritance and variable expression.

  1993cites this paper
• Median cleft of the lip: its significance and surgical repair.

  1993cites this paper
• Five cases of DeMyer sequence: an interophthalmic dysplasia.

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

  1991cites this paper
• Selected clinical research involving the central nervous system.

  1990cites this paper
• Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly.

  1989cites this paper
• Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities.

  1989cites this paper
• Case report and delineation of the congenital hypothalamic hamartoblastoma syndrome (Pallister-Hall syndrome).

  1989cites this paper