chromosomally < chromosome < chromosomes

Facettes : Author.f AffOrg.f AffPays.f AffRegion.f AffVille.f

List of bibliographic references

Number of relevant bibliographic references: 83.
[40-60] [0 - 20][0 - 50][60-80]

Ident.	Authors (with country if any)	Title
004741 (1995)	Tsutomu Ogata [Japon] ; Nobutake Matsuo [Japon]	Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features
004781 (1995)	Venkataraman N. Yang [Corée du Sud] ; Jae Sung Cho [Corée du Sud] ; Hae Won Min [Corée du Sud] ; Chang Hoon Lee [Corée du Sud] ; Chan Ho Song [Corée du Sud]	Rapid Chromosome Analysis and Prenatal Diagnosis Using Fluid from the Cystic Hygroma, Hydrothorax and Isolated Ascites: New Source for Chromosome Analysis
004792 (1995)	A. Villa [Espagne] ; M. Urioste ; M. C. Carrascosa [Espagne] ; S. Vázquez [Espagne] ; A. Martínez [Espagne] ; M. L. Martínez-Frías [Espagne]	Pericentric inversions of chromosome 4: report of a new family and review of the literature
004817 (1995)	Jean-Pierre Fryns [Belgique]	Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13
004894 (1995)	Beatriz Crispino [Uruguay] ; Horacio Cardoso [Uruguay] ; Adriana Mimbacas [Uruguay] ; Virginia Méndez [Uruguay]	Deletion of chromosome 3 and a 3;20 reciprocal translocation demonstrated by chromosome painting
004B13 (1994)	Anton Hsu [États-Unis]	Phenotype/Karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases
004E95 (1993)	F. Shabtai [Israël] ; E. Ben-Sasson [Israël] ; S. Arieli [Israël] ; J. Grinblat [Israël]	Chromosome 20 long arm deletion in an elderly malformed man.
005034 (1992)	Daniel L. Van Dyke ; Anne Wiktor ; Catherine G. Paliner ; Dorothy A. Miller ; Michal Witt [Pologne] ; V. Ramesh Babu ; Maria J. Worsham ; Jacquelyn R. Roberson ; Lester Weiss	Ullrich‐Turner syndrome with a small ring X chromosome and presence of mental retardation
005095 (1992)	Ulrich Wolf [Allemagne] ; Werner Schempp [Allemagne] ; Gerd Scherer [Allemagne]	Molecular biology of the human Y chromosome
005096 (1992)	V. Petrovic [Australie] ; S. Nasioulas [Australie] ; C W Chow [Australie] ; L. Voullaire [Australie] ; M. Schmidt [Australie] ; H. Dahl [Australie]	Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies.
005637 (1990)	Shinichi Miyabara [Japon]	Animal Model for Congenital Anomalies Induced by Chromosome Aberrations
005723 (1989)	M. Tyrkus [États-Unis] ; W. H. Hoffman [États-Unis] ; K. M. Kraemer-Flynn [États-Unis]	X chromosome instability associated with familial Turner syndrome
005727 (1989)	Natalie Blagowidow [États-Unis] ; David C. Page ; Dale Huff [États-Unis] ; Michael T. Mennuti [États-Unis]	Ullrich‐Turner syndrome in an XY female fetus with deletion of the sex‐determining portion of the Y chromosome
005784 (1989)	Michael A. Cantrell [États-Unis] ; James N. Bicknell [États-Unis] ; Roberta A. Pagon [États-Unis] ; David C. Page [États-Unis] ; David C. Walker [États-Unis] ; Howard M. Saal [États-Unis] ; Arthur B. Zinn [États-Unis] ; Christine M. Disteche [États-Unis]	Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe
005836 (1989)	Charlotte Ferencz [États-Unis] ; Catherine A. Neill [États-Unis] ; Joann A. Boughman [États-Unis] ; Judith D. Rubin [États-Unis] ; Joel I. Brenner [États-Unis] ; Lowell W. Perry [États-Unis]	Congenital cardiovascular malformations associated with chromosome abnormalities: An epidemiologic study
005B68 (1987)	M. Holmes-Siedle [Royaume-Uni] ; M. Ryynanen [Royaume-Uni, Finlande] ; R. H. Lindenbaum [Royaume-Uni]	Parental decisions regarding termination of pregnancy following prenatal detection of sex chromosome abnormality
005D27 (1986)	Walter P. Donlan [États-Unis] ; Cynthia R. Dolan [États-Unis] ; John M. Opitz [États-Unis] ; James F. Reynolds [États-Unis]	Ring chromosome 18 in a mother and son
005F25 (1985)	Felissa L. Cohen ; Jerry Dean Durham	Sex Chromosome Variations in School‐Age Children
005F52 (1985)	M N Daniel ; Linda Ekblom ; Sandra Phillips ; Joan M. Fitzgerald ; John M. Opitz ; Vincent M. Riccardi	NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome
006144 (1984)	Franca Anglani [Italie] ; Carlo Baccichetti [Italie] ; Lina Artifoni [Italie] ; Elisabetta Lenzini [Italie] ; Romano Tenconi [Italie]	Frequency of abnormal karyotypes in relation to the ascertainment method in females referred for suspected sex chromosome abnormality
006155 (1984)	N. Michels [États-Unis] ; Carol Lynn Berseth [États-Unis] ; John F. O'Brien [États-Unis] ; Gordon Dewald [États-Unis] ; John M. Opitz	Duplication of part of chromosome 1q: Clinical report and review of literature

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