104 related articles for article (PubMed ID: 7120317)
1. An unusual form of familial acrocephalosyndactyly.
Young ID; Harper PS
J Med Genet; 1982 Aug; 19(4):286-8. PubMed ID: 7120317
[TBL] [Abstract][Full Text] [Related]
2. Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child.
Soekarman D; Fryns JP; van den Berghe H
Genet Couns; 1992; 3(4):217-20. PubMed ID: 1472357
[TBL] [Abstract][Full Text] [Related]
3. [Acrocephalosyndactyly I (Apert syndrome)].
Linss G
Hautarzt; 2000 Sep; 51(9):685-7. PubMed ID: 11057397
[TBL] [Abstract][Full Text] [Related]
4. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes.
Robin NH; Segel B; Carpenter G; Muenke M
Am J Med Genet; 1996 Mar; 62(2):184-91. PubMed ID: 8882401
[TBL] [Abstract][Full Text] [Related]
5. Linkage analysis in dominant acrocephalosyndactyly.
Eastman JR; Escobar V; Bixler D
J Med Genet; 1978 Aug; 15(4):292-3. PubMed ID: 712761
[TBL] [Abstract][Full Text] [Related]
6. The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.
Brueton LA; van Herwerden L; Chotai KA; Winter RM
J Med Genet; 1992 Oct; 29(10):681-5. PubMed ID: 1433226
[TBL] [Abstract][Full Text] [Related]
7. Familial comedones. Evidence for autosomal dominant inheritance.
Cantú JM; Gómez-Bustamente MO; González-Mendoza A; Sánchez-Corona J
Arch Dermatol; 1978 Dec; 114(12):1807-9. PubMed ID: 153732
[TBL] [Abstract][Full Text] [Related]
8. [Acrocephaly, cranial asymmetry, brachydactyly, syndactyly, progressive senile dementia--a new type of acrocephalosyndactyly?].
Bukhanovskiĭ AO; Kit'ian VA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(5):688-92. PubMed ID: 6880496
[TBL] [Abstract][Full Text] [Related]
9. Familial neonatal and infantile seizures: an autosomal-dominant disorder.
Zonana J; Silvey K; Strimling B
Am J Med Genet; 1984 Jul; 18(3):455-9. PubMed ID: 6476007
[TBL] [Abstract][Full Text] [Related]
10. Acrocephalosyndactyly type 3: Chotzen's syndrome.
Bartsocas CS; Weber AL; Crawford JD
J Pediatr; 1970 Aug; 77(2):267-72. PubMed ID: 4393456
[No Abstract] [Full Text] [Related]
11. [Ocular manifestations during acrocephalosyndactyly (Apert's disease) (with presentation of 2 more cases)].
Melodia C; Belmonte M
Riv Otoneurooftalmol; 1969; 44(2):153-67. PubMed ID: 5356135
[No Abstract] [Full Text] [Related]
12. Familial inheritance of coronal craniosynostosis.
Kosnik EJ; Gilbert G; Sayers MP
Dev Med Child Neurol; 1975 Oct; 17(5):630-3. PubMed ID: 1183742
[TBL] [Abstract][Full Text] [Related]
13. Male transmission of Apert syndrome.
Rollnick BR
Clin Genet; 1988 Feb; 33(2):87-90. PubMed ID: 3359672
[TBL] [Abstract][Full Text] [Related]
14. An unusual familial muscle disorder.
Cumming WJ; Kristmundsdottir F; Mahon M
J Neurol Neurosurg Psychiatry; 1989 Feb; 52(2):266-9. PubMed ID: 2703844
[TBL] [Abstract][Full Text] [Related]
15. Phenotype definition and recurrence risk in the acrocephalosyndactyly syndromes.
Bull MJ; Escobar V; Bixler D; Antley RM
Birth Defects Orig Artic Ser; 1979; 15(5B):65-74. PubMed ID: 526591
[No Abstract] [Full Text] [Related]
16. A family with the Saethre-Chotzen syndrome.
Bianchi E; Aricŏ M; Podestă AF; Grana M; Fiori P; Beluffi G
Am J Med Genet; 1985 Dec; 22(4):649-58. PubMed ID: 4073118
[TBL] [Abstract][Full Text] [Related]
17. Acrocephalosyndactyly and partial trisomy 6.
Robertson KP; Thurmon TF; Tracy MC
Birth Defects Orig Artic Ser; 1975; 11(5):267-71. PubMed ID: 1240777
[TBL] [Abstract][Full Text] [Related]
18. [Acrocephalopolysyndactyly (type II (McKusick) acrocephalosyndactyly or Carpenter's syndrome. Report on 4 cases and an observation of the syndrome of Marshall-Smith (author's transl)].
Pfeiffer RA; Seemann KB; Tünte W; Gussone J; Klemm E
Klin Padiatr; 1977 Mar; 189(2):120-30. PubMed ID: 558466
[TBL] [Abstract][Full Text] [Related]
19. [Type V acrocephalosyndactylia (Pfeiffer's syndrome). Apropos of 3 cases in the same family].
Manouvrier-Hanu S; Herbaux B; Pellerin P; Douchet P; Bouchez-Bonniere MC; Dubos JP; Farriaux JP
Arch Fr Pediatr; 1989; 46(6):433-7. PubMed ID: 2783004
[TBL] [Abstract][Full Text] [Related]
20. Variable expression in Pfeiffer syndrome.
Sanchex HM; De Negrotti TC
J Med Genet; 1981 Feb; 18(1):73-5. PubMed ID: 7253005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]