Literature DB >> 2465411

18p- syndrome with partial sacral agenesis.

S Anderson-Shotwell, W G Wilson.   

Abstract

Mesh：

Year:  1989        PMID： 2465411      PMCID： PMC1015548          DOI： 10.1136/jmg.26.1.70

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  International system for human gene nomenclature (1979) ISGN (1979).

Authors:  T B Shows; C A Alper; D Bootsma; M Dorf; T Douglas; T Huisman; S Kit; H P Klinger; C Kozak; P A Lalley; D Lindsley; P J McAlpine; J K McDougall; P Meera Khan; M Meisler; N E Morton; J M Opitz; C W Partridge; R Payne; T H Roderick; P Rubinstein; F H Ruddle; M Shaw; J W Spranger; K Weiss
Journal:  Cytogenet Cell Genet       Date:  1979

2.  A genetic nomenclature for human blood coagulation.

Authors:  J B Graham; D A Barrett; B Blombäck; H M Cann; R M Hardisty; M J Larrieu; J H Renwick
Journal:  Thromb Diath Haemorrh       Date:  1973-09-15

3.  18p - syndrome with a single central maxillary incisor.

Authors:  L M Dolan; K Willson; W G Wilson
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318
  3 in total
  1 in total

Review 1.  Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.

Authors:  Gabriel C Dworschak; Heiko M Reutter; Michael Ludwig
Journal:  Orphanet J Rare Dis       Date:  2021-04-09       Impact factor: 4.123
  1 in total

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