Literature DB >> 14002918

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.

J J YUNIS, R J GORLIN.   

Abstract

Entities:  

Keywords:  CARCINOMA, BASAL CELL; CHROMOSOMES; DENTIGEROUS CYST; GENETICS, HUMAN; JAWS; RIBS

Mesh：

Year:  1963        PMID： 14002918     DOI： 10.1007/bf00336756

Source DB:  PubMed          Journal:  Chromosoma        ISSN： 0009-5915            Impact factor:   4.316


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  4 in total

1.  Multiple nevoid basal cell carcinoma, odontogenic keratocysts and skeletal anomalies. A syndrome.

Authors:  R J Gorlin; J J Yunis; N Tuna
Journal:  Acta Derm Venereol       Date:  1963       Impact factor: 4.437

2.  Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome.

Authors:  R J GORLIN; R W GOLTZ
Journal:  N Engl J Med       Date:  1960-05-05       Impact factor: 91.245

3.  The identification of individual chromosomes, especially in man.

Authors:  K PATAU
Journal:  Am J Hum Genet       Date:  1960-09       Impact factor: 11.025

4.  Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.

Authors:  K PATAU; E THERMAN; S L INHORN; D W SMITH; A L RUESS
Journal:  Chromosoma       Date:  1961       Impact factor: 4.316
  4 in total
  15 in total

1.  A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.

Authors:  H L COOPER; R HERNITS
Journal:  Am J Hum Genet       Date:  1963-12       Impact factor: 11.025

2.  IDENTIFICATION OF THE MONGOLISM CHROMOSOME BY DNA REPLICATION ANALYSIS.

Authors:  J J YUNIS; E B HOOK; M MAYER
Journal:  Am J Hum Genet       Date:  1965-05       Impact factor: 11.025

3.  A cytogenetic study of recurrent abortion.

Authors:  M K Bhasin; W Foerster; W Fuhrmann
Journal:  Humangenetik       Date:  1973-04-16

4.  Frequency and genetic effect of 1qh plus.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson
Journal:  Humangenetik       Date:  1974-02-21

5.  Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.

Authors:  H Van den Berghe; M Van Eygen; J P Fryns; W Tanghe; H Verresen
Journal:  Humangenetik       Date:  1973-05-25

6.  A familial variant of chromosome 9.

Authors:  C G Palmer; J Schroder
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

7.  The nevoid basal cell carcinoma syndrome.

Authors:  D E Anderson; W B Taylor; H F Falls; R T Davidson
Journal:  Am J Hum Genet       Date:  1967-01       Impact factor: 11.025

8.  [Multiple abnormalities in a girl with a 46, XY,17q+ karyotype].

Authors:  W Engel; H Reinwein; D Bombel; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1968

9.  [Elongated, submetacentric chromosome no. 1. A very rare heterozygote variant in man].

Authors:  B Saner
Journal:  Humangenetik       Date:  1970-08-17

10.  Probable pericentric inversion in chromosome no. 1 in a female child (46,XX,inv(Ip+q-).

Authors:  A V Mikelsaar; E V Ananjev; V M Gindilis
Journal:  Humangenetik       Date:  1970
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