Karyotype 47, XXY,18p- in a newborn child with holoprosencephaly-Reference-Cited by-同舟云学术

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Karyotype 47, XXY,18p- in a newborn child with holoprosencephaly

Published:2008-04-23 Issue:3 Volume:23 Page:186-190
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Schnabel R.,Hansen S.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1983.tb01870.x/fullpdf

Reference16 articles.

1. Megalencephaly and chromosomal anomaly;Budka;Acta neuropath.,1978

2. Presumptive deletion of the short arms of chromosome 18 in a cyclops;Faint;Hum. Chrom. Newsl.,1964

3. Short arm deletion of chromosome 18 in cebocephaly;Gorlin;Amer. J. Dis. Child.,1968

4. Descriptive neuropathology of chromosomal disorders in man;Gullotta;Hum. Genet.,1981

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother;Taiwanese Journal of Obstetrics and Gynecology;2012-12

2. Nase und Nasennebenhöhlen;Spezielle pathologische Anatomie;1999

3. Holoprosencephaly: A developmental field defect;American Journal of Medical Genetics;1989-10

4. Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly;American Journal of Medical Genetics;1989-10

5. Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities;American Journal of Medical Genetics;1989-10

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