Literature DB >> 8487277

Otopalatodigital syndrome type II.

S E Holder1, R M Winter.   

Abstract

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Year:  1993        PMID: 8487277      PMCID: PMC1016340          DOI: 10.1136/jmg.30.4.310

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


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  13 in total

1.  Oto-Palato-Digital syndrome with severe X-ray changes in two half brothers.

Authors:  K Kozlowski; G Turner; J Scougall; J Harrington
Journal:  Pediatr Radiol       Date:  1977-09-01

2.  A familial syndrome of cranial, facial, oral and limb anomalies.

Authors:  N Fitch; S Jequier; A Papageorgiou
Journal:  Clin Genet       Date:  1976-10       Impact factor: 4.438

3.  Oto-palato-digital syndrome, type II: evidence for defective intramembranous ossification.

Authors:  T Ogata; N Matsuo; G Nishimura; H Hajikano
Journal:  Am J Med Genet       Date:  1990-06

4.  Melnick-Needles syndrome in males.

Authors:  M Krajewska-Walasek; J Winkielman; R J Gorlin
Journal:  Am J Med Genet       Date:  1987-05

5.  Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.

Authors:  J C Gall; A M Stern; A K Poznanski; S M Garn; E D Weinstein; J R Hayward
Journal:  Am J Hum Genet       Date:  1972-01       Impact factor: 11.025

6.  The oto-palato-digital syndrome, proposed type II.

Authors:  N Fitch; S Jequier; R Gorlin
Journal:  Am J Med Genet       Date:  1983-08

7.  Abnormal facies, cleft palate, and generalized dysostosis: a lethal X-linked syndrome.

Authors:  M André; J Vigneron; F Didier
Journal:  J Pediatr       Date:  1981-05       Impact factor: 4.406

8.  The roentgenographic features of the oto-palato-digital (OPD) syndrome.

Authors:  L O Langer
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1967-05

9.  Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasia.

Authors:  T G Brewster; R S Lachman; D C Kushner; L B Holmes; R J Isler; D L Rimoin
Journal:  Am J Med Genet       Date:  1985-02

10.  Cleidocranial dysostosis, severe micrognathism, bilateral absence of thumbs and first metatarsal bone, and distal aphalangia: a new genetic syndrome.

Authors:  E Yunis; H Varón
Journal:  Am J Dis Child       Date:  1980-07
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  1 in total

1.  Asphyxiating thoracic dystrophy with facial dysmorphism.

Authors:  V H Sankar; Shubha R Phadke
Journal:  Indian J Pediatr       Date:  2006-12       Impact factor: 1.967

  1 in total

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