Literature DB >> 14215563

RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISM.

R R GORDON, P COOKE.   

Abstract

Entities:  

Keywords:  CHROMOSOME ABNORMALITIES; DWARFISM; INFANT; INFANT, NEWBORN; MICROCEPHALY

Mesh:

Year:  1964        PMID: 14215563     DOI: 10.1016/s0140-6736(64)91045-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  15 in total

1.  Clinical consequences of deletion 1p35.

Authors:  S L Wenger; M W Steele; D J Becker
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

Review 2.  Monosomy 1p36.

Authors:  A Slavotinek; L G Shaffer; S K Shapira
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

3.  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

4.  Multiple congenital anomalies associated with a ring-D chromosome.

Authors:  R C Juberg; M S Adams; W J Venema; M G Hart
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

5.  Ring chromosomes in two infants with congenital malformations.

Authors:  M A Varela; W H Sternberg
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

6.  A large deletion of chromosome no. 1 (46,XY,1?--).

Authors:  D Aarskog
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

7.  Ring chromosome 18 in a patient with multiple anomalies.

Authors:  C G Palmer; N Fareed; A D Merritt
Journal:  J Med Genet       Date:  1967-06       Impact factor: 6.318

8.  An infant with multiple congenital anomalies and a ring chromosome in group C (X-6-12).

Authors:  L J Butler; N E France; N M Jacoby
Journal:  J Med Genet       Date:  1967-12       Impact factor: 6.318

9.  Terminal deletion of (1)(q42) and its phenotypical manifestations.

Authors:  M Andrle; A Erlach; W R Mayr; A Rett
Journal:  Hum Genet       Date:  1978-02-23       Impact factor: 4.132

10.  Terminal deletion of the long arm of chromosome 1 in a malformed newborn.

Authors:  E Kessel; R A Pfeiffer; W Blanke; J Schwarz
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132

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