Literature DB >> 5653872

Arrhinencephaly associated with a deficiency involving chromosome 18.

A McDermott, J Insley, M E Barton, P Roowe, J H Edwards, A H Cameron.   

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Year:  1968        PMID： 5653872      PMCID： PMC1468608          DOI： 10.1136/jmg.5.1.60

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


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  10 in total

1.  PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Authors:  H E VANDYKE; A VALDMANIS; J D MANN
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

2.  A 46 CHROMOSOME CEBOCEPHALY, WITH REMARKS ON THE RELATION OF 13-15 TRISOMY TO HOLOPROSENCEPHALY (ARHINENCEPHALY).

Authors:  W DEMYER
Journal:  Ann Paediatr       Date:  1964

3.  DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Authors:  R L SUMMITT
Journal:  Cytogenetics       Date:  1964

4.  FAMILIAL ALOBAR HOLOPROSENCEPHALY (ARHINENCEPHALY) WITH MEDIAN CLEFT LIP AND PALATE. REPORT OF PATIENT WITH 46 CHROMOSOMES.

Authors:  W DEMYER; W ZEMAN; C D PALMER
Journal:  Neurology       Date:  1963-11       Impact factor: 9.910

5.  FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors:  I A UCHIDA; K N MCRAE; M RAY
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

6.  Arhinencephaly.

Authors:  J W LANDAU; J M BARRY; R KOCH
Journal:  J Pediatr       Date:  1963-06       Impact factor: 4.406

7.  Cyclopian-type malformation in lambs.

Authors:  W BINNS; L F JAMES; J L SHUPE; E J THACKER
Journal:  Arch Environ Health       Date:  1962-08

8.  Cebocephaly with endocrine dysgenesis. Report of 3 cases.

Authors:  J C HAWORTH; H MEDOVY; A J LEWIS
Journal:  J Pediatr       Date:  1961-11       Impact factor: 4.406

9.  [Exclusion of certain autosomal localizations of blood and serum group genes].

Authors:  C Salmon; C Ropartz; J de Grouchy; J Lejeune; D Salmon; L Rivat; P Y Rousseau; F Delarue; G Liberge
Journal:  Ann Genet       Date:  1966

10.  The "D" (13-15) trisomy syndrome: an analysis of 7 examples.

Authors:  G J Snodgrass; L J Butler; N E France; L Crome; A Russell
Journal:  Arch Dis Child       Date:  1966-06       Impact factor: 3.791
  10 in total
  13 in total

1.  A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent.

Authors:  G Johnson; R Bachman
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

5.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

6.  Absent IgA and deletions of chromosome 18.

Authors:  J M Stewart; S Go; E Ellis; A Robinson
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

7.  Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.

Authors:  P Fischer; E Golob; F Friedrich; E Kunze-Mühl; W Doleschel; H Aichmair
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

8.  A patient with a short arm deletion of chromosome 18 (46,XY,18p-).

Authors:  L Weiss; K Mayeda
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

9.  A case of suspected teratogenic holoprosencephaly.

Authors:  M Stabile; A Bianco; S Iannuzzi; M C Buonocore; V Ventruto
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

10.  Descriptive neuropathology of chromosomal disorders in man.

Authors:  F Gullotta; H Rehder; A Gropp
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
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