Identical twins discordant for Kallmann's syndrome.

No abstract is available for this paper.

• Publication year

  1990

• Venue

  Journal of Medical Genetics

• Publication date

  1990-03-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1136/jmg.27.3.198PMID 2325096PMCID PMC1017005
• 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.

• [Monozygotic twins with schizoform psychosis and hypothalamic-induced hypogonadotropic hypogonadism].

  1987cited by this paper
• Heterogeneity of Kallmann's syndrome

  1985cited by this paper
• Hypogonadotropic hypogonadism associated with retinitis pigmentosa in a female sibship: evidence for gonadotropin deficiency.

  1981cited by this paper
• Maladie de Parkinson et anosmie chez deux jumelles monozygotiques

  1976cited by this paper
• [Parkinson's disease and anosmia in monozygotic twin sisters (author's transl)].

  1976cited by this paper
• Hypogonadotropic eunuchoidism. I. Clinical study of the mode of inheritance.

  1973cited by this paper
• Book Review: The Metabolic Basis of Inherited Disease

  1967cited by this paper
• The genetic aspects of primary eunuchoidism

  1944cited by this paper

• Врожденный изолированный гипогонадотропный гипогонадизм: клинический и молекулярно-генетический полиморфизм

  2021cites this paper
• Combined in vitro and in silico analyses of FGFR1 variants: genotype‐phenotype study in idiopathic hypogonadotropic hypogonadism

  2020cites this paper
• Delayed Puberty

  2020cites this paper
• Next-generation sequencing of patients with congenital anosmia

  2017cites this paper
• Molecular Genetics of Kallmann Syndrome and Constitutional delay of growth and puberty in Finland

  2014cites this paper
• Chapter 16 – Twins and Twinning

  2013cites this paper
• Invertebrate Models of Kallmann Syndrome: Molecular Pathogenesis and New Disease Genes

  2013cites this paper
• Syndrome de Kallmann (KS) : étude de corrélation phénotype/génotype et des modes de transmission de mutations PROK2 et PROKR2 : caractérisation d’un nouveau gène responsable de KS, l’alpha dystrobrévine

  2012influential citation
• Isolated GnRH deficiency: a disease model serving as a unique prism into the systems biology of the GnRH neuronal network.

  2011cites this paper
• CHAPTER 25 – Puberty: Ontogeny, Neuroendocrinology, Physiology, and Disorders

  2011cites this paper
• Identical But Not the Same : The Value of Discordant Monozygotic Twins in Genetic Research

  2010cites this paper
• Clinical genetics of Kallmann syndrome.

  2010cites this paper
• Identical but not the same: The value of discordant monozygotic twins in genetic research

  2010cites this paper
• Biological actions and interactions of anosmin-1.

  2010cites this paper
• Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism.

  2009cites this paper
• Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism.

  2009cites this paper
• The Complex Genetics of Kallmann Syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.

  2008cites this paper
• The Complex Genetics of Kallmann Syndrome : KAL 1 , FGFR 1 , FGF 8 , PROKR 2 , PROK

  2008cites this paper
• Síndrome de Kallmann: uma revisão histórica, clínica e molecular

  2008cites this paper
• [Kallmann syndrome: a historical [corrected] clinical and molecular review].

  2008cites this paper
• Kallmann syndrome

  2007cites this paper
• Diversity in Fibroblast Growth Factor Receptor 1 Regulation: Learning from the Investigation of Kallmann Syndrome

  2007cites this paper
• Reversible Kallmann syndrome: report of the first case with a KAL1 mutation and literature review.

  2007cites this paper
• Hypogonadisme hypogonadotrophique congénital: procréation, grossesses et descendance

  2007cites this paper
• Kallmann syndrome: fibroblast growth factor signaling insufficiency?

  2004cites this paper
• Hypogonadismes hypogonadotrophiques chez l'homme

  2004cites this paper
• The genetics of IHH–a paradox *

  2001cites this paper
• Kallmann syndrome: towards molecular pathogenesis.

  2001cites this paper
• Hypogonadismes hypogonadotrophiques chez l'homme

  2000cites this paper
• A novel mutation of the KAL1 gene in monozygotic twins with Kallmann syndrome.

  2000cites this paper
• Luteinizing hormone‐releasing hormone and innervation pathways in human prenatal nasal submucosa: factors of importance in evaluating Kallmann's syndrome

  1996cites this paper
• Twins and twinning.

  1996cites this paper
• X-linked Kallmann's syndrome : a molecular genetic and developmental analysis.

  1996cites this paper
• A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndrome.

  1995cites this paper
• Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene.

  1995cites this paper
• Comments on discordant monozygotic twinning in homosexuality

  1994cites this paper
• The Kallmann's syndrome variant (KSV) model of the schizophrenias.

  1993cites this paper
• Disorders of puberty in boys.

  1993cites this paper
• Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type

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

  1991cites this paper