Literature DB >> 13776246

The D triisomy syndrome and XO gonadal dysgenesis in two sisters.

E THERMAN, K PATAU, D W SMITH, R I DEMARS.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; TURNER'S SYNDROME/genetics

Mesh：

Year:  1961        PMID： 13776246      PMCID： PMC1932116     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  13 in total

1.  The chromosomes in a patient showing both mongolism and the Klinefelter syndrome.

Authors:  C E FORD; K W JONES; O J MILLER; U MITTWOCH; L S PENROSE; M RIDLER; A SHAPIRO
Journal:  Lancet       Date:  1959-04-04       Impact factor: 79.321

2.  A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

Authors:  C E FORD; K W JONES; P E POLANI; J C DE ALMEIDA; J H BRIGGS
Journal:  Lancet       Date:  1959-04-04       Impact factor: 79.321

3.  A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome.

Authors:  D W SMITH; K PATAU; E THERMAN; S L INHORN
Journal:  J Pediatr       Date:  1960-09       Impact factor: 4.406

4.  Chromosomal trisomy associated with the Sturge-Weber syndrome.

Authors:  M D HAYWARD; B D BOWER
Journal:  Lancet       Date:  1960-10-15       Impact factor: 79.321

5.  Human chromosome complements in normal somatic cells in culture.

Authors:  E H CHU; N H GILES
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

6.  A new trisomic syndrome.

Authors:  J H EDWARDS; D G HARNDEN; A H CAMERON; V M CROSSE; O H WOLFF
Journal:  Lancet       Date:  1960-04-09       Impact factor: 79.321

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

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

8.  The Klinefeltermongolism type of double aneuploidy.

Authors:  D G HARNDEN; O J MILLER; L S PENROSE
Journal:  Ann Hum Genet       Date:  1960-05       Impact factor: 1.670

9.  THE SOMATIC CHOMOSOMES OF MAN.

Authors:  J H Tjio; T T Puck
Journal:  Proc Natl Acad Sci U S A       Date:  1958-12-15       Impact factor: 11.205

10.  Genetics of somatic mammalian cells. II. Chromosomal constitution of cells in tissue culture.

Authors:  J H TJIO; T T PUCK
Journal:  J Exp Med       Date:  1958-08-01       Impact factor: 14.307
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  23 in total

1.  TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Authors:  W E NANCE; I UCHIDA
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

2.  [Chromosome anomalies in the blood cells of a child with multiple abnormalities].

Authors:  R A PFEIFFER; G SCHELLONG; W KOSENOW
Journal:  Klin Wochenschr       Date:  1962-10-15

3.  Dermal patterns of 18 and D1 trisomics.

Authors:  I A UCHIDA; K PATAU; D W SMITH
Journal:  Am J Hum Genet       Date:  1962-12       Impact factor: 11.025

4.  Multiple developmental anomalies and trisomy of a 13-15 group chromosome ('D' syndrome).

Authors:  P E CONEN; K G PHILLIPS; L S MAUNTNER
Journal:  Can Med Assoc J       Date:  1962-09-29       Impact factor: 8.262

5.  An XYY man with progeny indicating familial tendency to non-disjunction.

Authors:  T S HAUSCHKA; J E HASSON; M N GOLDSTEIN; G F KOEPF; A A SANDBERG
Journal:  Am J Hum Genet       Date:  1962-03       Impact factor: 11.025

6.  Trisomy for chromosome No. 18 in man.

Authors:  K PATAU; E THERMAN; D W SMITH; R I DEMARS
Journal:  Chromosoma       Date:  1961       Impact factor: 4.316

7.  Partial-trisomy syndromes. I. Sturge-Weber's disease.

Authors:  K PATAU; E THERMAN; D W SMITH; S L INHORN; B F PICKEN
Journal:  Am J Hum Genet       Date:  1961-09       Impact factor: 11.025

8.  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

9.  Diverse chromosomal anomalies in a family.

Authors:  L Atkins; C S Bartsocas; P J Porter
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

Review 10.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971
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