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Serveur d'exploration sur le lymphœdème - Curation (Ncbi)

Index « Keywords » - entrée « Chromosome Disorders »
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Chromosome Deletion < Chromosome Disorders < Chromosome Disorders (complications)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 16.
Ident.Authors (with country if any)Title
000564 (2001) Y. Fatinni [Arabie saoudite] ; A. Asindi ; Y. Al Falki ; A. Al Harthi ; S. Al Fifi ; S. Al-DaamaPossible new autosomal recessive syndrome of congenital lymphoedema, nail dystrophy and esotropia in a Saudi family.
000B96 (2003) Brad Angle [États-Unis] ; Frank Yen ; Joseph H. Hersh ; Gordon GowansPatient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.
001567 (1965) P. F. Benson ; M. H. Gough ; P. E. PolaniLymphangiography and Chromosome Studies in Females with Lymphoedema and Possible Ovarian Dysgenesis
002540 (????) C. Severien ; S. Felix ; K. BartholoméRing chromosome 22: a case report.
002A14 (1991) D. Lacombe [France] ; A. Taieb ; P. Masson ; M. Fayon ; J L DemarquezNeonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.
002D40 (2008) Kavita Radhakrishnan [États-Unis] ; Stanley G. RocksonThe clinical spectrum of lymphatic disease.
007598 (1989) D D Farhud ; I. Farhud ; G R Walizadeh ; M. Djaber-AnsariCongenital hereditary lymphedema (Nonne/Milroy).
009498 (1986) H J Voigt ; U. Claussen ; R. Ulmer[Fetal neck edema--early sonographic indications of a chromosome abnormality].
009A51 (1986) A H Salem ; A M Mulhim ; C. Grant ; M S KhwajaMilroy's disease in a Saudi family.
009B86 (1985) L W Terstappen ; R P Arens ; C H Ten Napel[Hereditary lymphedema, a frequently unrecognized form of chronic edema; clinical study in 2 families with Meige's disease].
009D32 (1967) P F Benson ; A I Taylor ; M H GoughChromosome anomalies in primary lymphoedema.
009F66 (1972) E W PriceA possible genetic factor in non-filarial elephantiasis of the lower legs.
00A829 (????) M. Burdea ; C. Belinschi ; A. Harmanschi ; O. Rusu[Turner's syndrome with karyotype XO associated with the Debré-Fibiger syndrome].
00A941 (1981) R. Henrion ; M C Aubry ; J P Aubry ; C N Emmanuelli ; Y. Dumez ; J F Oury[The antenatal diagnosis of Bonnevie-Ullrich's syndrome. The role of ultrasound (author's transl)].
00AB58 (1978) L B Holmes ; J P Fields ; J B ZabriskieHereditary late-onset lymphedema.
00AD03 (????) H R Mendoza[A peculiar syndrome of congenital abnormalities].

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