47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

Human genetics ·Vol. 31 ·No. 3 ·1976-03-12 ·Pages 271-82

Fujita H, Shimazaki M, Takeuchi T, Hayakawa Y, Oura T

Abstract

Marker chromosomes carried by unrelated 3 cases were identified as a part of No. 9 chromosome through the analysis of the chromatid fine structure after trypsin-giemsa treatment. They showed characteristic features of that 9p trisomic syndrome which were described by Rethoré et al. (1973). In addition to those features, some clinical and laboratory findings on growth hormon deficiency were disclosed in this report.

MeSH Terms

Child Child, Preschool Chromosomes, Human, 6-12 and X Dermatoglyphics Dwarfism, Pituitary/genetics Female Growth Growth Hormone/deficiency,metabolism Humans Infant Male Phenotype Pituitary Function Tests Trisomy

Chemicals

Growth Hormone

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Fujita H

Shimazaki M

Takeuchi T

Hayakawa Y

Oura T

References (12)

12 references, click to expand

[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
Ann Genet. 1970 Dec;13(4):217-32 PMID: 5313386
[Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].
Z Kinderheilkd. 1971;109(4):293-9 PMID: 5555168
[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].
Ann Genet. 1966;9(1):12-8 PMID: 5295698
Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.
Humangenetik. 1974;25(2):83-92 PMID: 4140843
Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).
Humangenetik. 1975;27(3):269-74 PMID: 1150249
A case of trisomy 9p in a family with translocation 9/15.
Humangenetik. 1975;27(4):353-8 PMID: 1150257
Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
J Pediatr. 1974 Jul;85(1):92-5 PMID: 4855265
Banding in human chromosomes treated with trypsin.
Nat New Biol. 1972 Jan 12;235(54):52-4 PMID: 4109406
Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
Humangenetik. 1971;12(3):175-81 PMID: 5563410
A new case of trisomy for the short arm of No. 9 chromosome.
J Med Genet. 1973 Sep;10(3):296-9 PMID: 4774540
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
Humangenetik. 1973 Apr 16;18(2):129-38 PMID: 4124236
[Cp trisomy: a new syndrome].
Ann Genet. 1971 Sep;14(3):177-86 PMID: 5315464

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00270857

Published

1976-03-12

Pages

271-82

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00270857 View journal details

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47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

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