Literature DB >> 14097240

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

H L COOPER, R HERNITS.   

Abstract

Entities:  

Keywords:  BLOOD GROUPS; CHROMOSOME ABNORMALITIES; HAPTOGLOBINS; HERMAPHRODITISM

Mesh:

Substances:

Year:  1963        PMID: 14097240      PMCID: PMC1932555     

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


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  3 in total

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

Authors:  J J YUNIS; R J GORLIN
Journal:  Chromosoma       Date:  1963       Impact factor: 4.316

2.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

3.  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

  3 in total
  16 in total

1.  A cytogenetic study of recurrent abortion.

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

2.  Frequency and genetic effect of 1qh plus.

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

3.  [Polymorphism of human constitutive heterochromatin in metaphase chromosome A1].

Authors:  M A Kim
Journal:  Humangenetik       Date:  1973-05-25

4.  Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication.

Authors:  J R Lobitz; B K McCaw; F Hecht
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

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.  Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I.

Authors:  A D Merritt; E W Lovrien; M L Rivas; P M Conneally
Journal:  Am J Hum Genet       Date:  1973-09       Impact factor: 11.025

7.  A familial variant of chromosome 9.

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

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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