The 4p-syndrome, with a report of two new cases.

Humangenetik ·Vol. 19 ·No. 1 ·1973-00-00 ·Pages 99-109

Fryns JP, Eggermont E, Verresen H, Van den Berghe H

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Chromosome Aberrations/diagnosis Chromosome Disorders Chromosomes, Human, 4-5 Dermatoglyphics Humans Infant Infant, Newborn Intellectual Disability/genetics Karyotyping Male Microcephaly/genetics Syndrome

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Fryns J P

Eggermont E

Verresen H

Van den Berghe H

References (22)

22 references, click to expand

A syndrome of retarded development with characteristic appearance.
Am J Dis Child. 1968 Jun;115(6):698-702 PMID: 4297583
A ring-4 chromosome in a patient with normal intelligence and short stature.
J Med Genet. 1971 Dec;8(4):517-21 PMID: 5149537
[New documents of delineation of a syndrome of the deletion of the short arm of one chromosome no 4].
Z Kinderheilkd. 1968;102(1):49-61 PMID: 5303548
The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
Am J Dis Child. 1971 Nov;122(5):421-5 PMID: 5129531
[On a case of "crying cat" syndrome with peculiar phenotypic anomalies].
Minerva Pediatr. 1965 Dec 15;17(39):1972-5 PMID: 5860653
[Cytogenetic and pathological observations in the (4p-) SYNDROME (Wolf syndrome)].
Beitr Pathol. 1971 Apr;143(1):84-96 PMID: 5577069
Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.
Humangenetik. 1965;1(5):479-82 PMID: 5895684
[Hallermann-Streiff-François syndrome: a recent case associated with a karyotypic 4 p-anomaly].
Pediatrie. 1968 Sep;23(6):703-5 PMID: 5739927
Short-arm deletion, chromosome 4, (4p-), a syndrome?
Ann Hum Genet. 1970 Oct;34(2):137-44 PMID: 5493842
Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.
J Med Genet. 1970 Jun;7(2):164-70 PMID: 5519605
Mewing cry in a child with the partial deletion of the short arm of chromosome no. 4.
Humangenetik. 1969;8(3):242-8 PMID: 5391962
New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.
JAMA. 1967 Oct 30;202(5):434-7 PMID: 6072506
Congenital malformations associated with a ring 4 chromosome.
J Med Genet. 1969 Jun;6(2):224-7 PMID: 5801472
[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102 PMID: 14095841
Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome.
Cytogenetics. 1966;5(3):137-51 PMID: 5921496
Partial deletion of the short arm of a chromosome No. 4. Wolf's syndrome.
Maandschr Kindergeneeskd. 1967 Oct;35(8):252-69 PMID: 6065161
A complex chromosomal rearrangement with formation of a ring 4.
J Med Genet. 1971 Jun;8(2):235-9 PMID: 5096548
Human chromosomal deletion: two patients with the 4p- syndrome.
J Pediatr. 1970 Jan;76(1):82-8 PMID: 5410164
[Deficiency on the short arms of a chromosome No. 4].
Humangenetik. 1965;1(5):397-413 PMID: 5868696
Human chromosomal deficiency: the 4p--syndrome.
Humangenetik. 1970 Aug 17;10(1):51-7 PMID: 5449950
Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.
J Pediatr. 1970 Nov;77(5):792-801 PMID: 5504070
Deletion of short arm of no. 4 (4p-)--a detailed case report.
J Med Genet. 1970 Jun;7(2):171-6 PMID: 5519606

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00295238

Published

1973-00-00

Pages

99-109

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00295238

Analysis Services

The 4p-syndrome, with a report of two new cases.

Contact

WeChat Official Account