0009-8981 < 0009-9163 < 0009-9228

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List of bibliographic references

Number of relevant bibliographic references: 66.
[40-60] [0 - 20][0 - 50][60-65][60-80]

Ident.	Authors (with country if any)	Title
005380 (1991)	D. G. R. Evans	Dominantly inherited microcephaly, hypotelorism and normal intelligence
005386 (1991)	D. G. R. Evans [Royaume-Uni] ; R. N. Lonsdale ; M. A. Patton [Royaume-Uni]	Cutaneous lymphangioma and amegakaryocytic thrombocytopenia in Noonan syndrome
005413 (1991)	Silvia Castillo-Taucher ; Juan Pable Beca ; Raúl Sáez ; Ver Nica Geldres	Balanced pericentric inversion 8(p23q13) in a child with rhizomelic chondrodysplasia punctata and his mother
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
005B29 (1987)	H. Kawashima [Japon] ; N. Tsuji [Japon]	Syndrome of microcephaly, deafness/ malformed ears, mental retardation and peculiar facies in a mother and son
005C34 (1987)	Jonathan Treisman [États-Unis] ; Francis S. Collins [États-Unis]	Adult Turner syndrome associated with chylous ascites and vascular anomalies
005D62 (1986)	J. A. Delgado ; C. M. Trahms ; V. P. Sybert [États-Unis]	Measurement of body fat in Turner syndrome
005E31 (1986)	D. Urbach [Israël] ; M. Hertz [Israël] ; M. Shine [Israël] ; R. M. Goodman [Israël]	A new skeletal dysplasia syndrome with rhizomelia of the humeri and other malformations
005F97 (1985)		European Society of Human Genetics Abstracts from XVIII Symposium
006003 (1985)	Alexander K. C. Leung [Canada]	Dominantly inherited syndrome of microcephaly and congenital lymphedema
006139 (1984)	Helena K Ri Inen	Hereditary lymphedema: a new combination of symptoms not fitting into present classifications
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
006177 (1984)	Troels Lyngbye ; Hella Koopmann Kristensen ; Marie Bojsen-M Ller [Danemark]	Alpers' disease
006184 (1984)	P. K. A. Jensen [Danemark]	A 5p;22q reciprocal translocation with a high risk for segregation of unbalanced offspring
006235 (1983)	Gary Berkovitz [Venezuela, États-Unis] ; Judith Stamberg [Venezuela] ; Leslie P. Plotnick [Venezuela] ; Roberto Lanes [États-Unis]	Turner syndrome patients with a ring X chromosome
006410 (1982)	B. Goldman [Royaume-Uni] ; P. E. Polani [Royaume-Uni] ; M. G. Daker [Royaume-Uni] ; R. R. Aangel [Royaume-Uni]	Clinical and cytogenetic aspects of X‐chromosome deletions
006507 (1981)	F. G. Cassorla [États-Unis] ; B S. Emanuel [États-Unis] ; J. S. Parks [États-Unis] ; C. H. Wu [États-Unis] ; J. E. Wheeler [États-Unis] ; A. Tenore [États-Unis]	Cytogenetic and endocrine findings in a female with 45, X, t(Y;18) (p11;p11)
006588 (1980)	P. Vittay ; P. Bösze [Hongrie] ; Magdolna Gaál [Hongrie] ; J. Lászl	Lymph vessel defects in patients with ovarian dysgenesis
006679 (1979)	S. J. Funderburk [États-Unis] ; R. S. Sparkes [États-Unis] ; I. Klisak [États-Unis]	Phenotypic variation in two patients with a ring chromosome 22
006683 (1979)	Jane L. Burns [États-Unis] ; Judith G. Hall [États-Unis] ; Ellen Powers [États-Unis] ; James B. Callis [États-Unis] ; Holger Hoehn [États-Unis]	No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45 XO Turner syndrome
006699 (1979)	Harold N. Bass [États-Unis] ; Robert S. Sparkes [États-Unis] ; Alvin A. Miller [États-Unis]	Features of trisomy 18 and 18p‐syndromes in an infant with 46, XY, i(18q)

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