97 related articles for article (PubMed ID: 1642806)
1. Familial occurrence of Summitt syndrome or a variant example of Carpenter syndrome?
Pierquin G; Seligmann R; Van Regemorter N
Genet Couns; 1992; 3(2):101-5. PubMed ID: 1642806
[TBL] [Abstract][Full Text] [Related]
2. Carpenter syndrome: marked variability of expression to include the Summitt and Goodman syndromes.
Gershoni-Baruch R
Am J Med Genet; 1990 Feb; 35(2):236-40. PubMed ID: 2309763
[TBL] [Abstract][Full Text] [Related]
3. Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes.
Cohen DM; Green JG; Miller J; Gorlin RJ; Reed JA
Am J Med Genet; 1987 Oct; 28(2):311-24. PubMed ID: 3322002
[TBL] [Abstract][Full Text] [Related]
4. Normal intelligence in two children with Carpenter syndrome.
Frias JL; Felman AH; Rosenbloom AL; Finkelstein SN; Hoyt WF; Hall BD
Am J Med Genet; 1978; 2(2):191-9. PubMed ID: 263437
[TBL] [Abstract][Full Text] [Related]
5. [The problem of diagnosis and risk in cases of acrocephaly].
Predescu V; Christodorescu D
Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1975; 20(3):229-36. PubMed ID: 1085470
[No Abstract] [Full Text] [Related]
6. Carpenter syndrome: a case report.
Begum S; Khatun N; Rayhan SM; Rahman SA
Mymensingh Med J; 2012 Jul; 21(3):547-9. PubMed ID: 22828559
[TBL] [Abstract][Full Text] [Related]
7. Carpenter syndrome.
Hidestrand P; Vasconez H; Cottrill C
J Craniofac Surg; 2009 Jan; 20(1):254-6. PubMed ID: 19165041
[TBL] [Abstract][Full Text] [Related]
8. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents.
Richieri-Costa A; Pirolo Júnior L; Cohen MM
Am J Med Genet; 1993 Aug; 47(2):281-3. PubMed ID: 8213921
[TBL] [Abstract][Full Text] [Related]
9. Apert syndrome.
Suparta N; Hartono ; Sunartini
Paediatr Indones; 1991; 31(11-12):319-24. PubMed ID: 1845657
[TBL] [Abstract][Full Text] [Related]
10. [Familial acrocephalosyndactylia with features of the Saethre-Chotzen syndrome].
Kopyść Z; Kulczyk B; Ryzko J; Gura C; Stańska M; Kowalski K
Pediatr Pol; 1979 Jul; 54(7):769-72. PubMed ID: 530768
[No Abstract] [Full Text] [Related]
11. [Acrocephalosyndactylia--Vogt syndrome].
Fehlow P; Walther F
Psychiatr Neurol Med Psychol (Leipz); 1985 Jun; 37(6):323-9. PubMed ID: 4034800
[TBL] [Abstract][Full Text] [Related]
12. [Hereditary syndromes featuring oligophrenia and obesity].
Ustinova EV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(3):435-9. PubMed ID: 7020300
[No Abstract] [Full Text] [Related]
13. The Saethre-Chotzen syndrome.
Kreiborg S; Pruzansky S; Pashayan H
Teratology; 1972 Dec; 6(3):287-94. PubMed ID: 4643612
[No Abstract] [Full Text] [Related]
14. Carpenter syndrome: report of two siblings.
Işlek I; Küçüködük S; Incesu L; Selçuk MB; Aygün D
Clin Dysmorphol; 1998 Jul; 7(3):185-9. PubMed ID: 9689991
[TBL] [Abstract][Full Text] [Related]
15. Short stature, brachydactyly, small ears, and a pattern of minor anomalies in brother and sister born to consanguineous parents: a hitherto unreported syndrome?
Schinzel A; Bernasconi S
Am J Med Genet; 1990 Jun; 36(2):243-6. PubMed ID: 2368813
[TBL] [Abstract][Full Text] [Related]
16. Prenatal findings in carpenter syndrome and a novel mutation in RAB23.
Haye D; Collet C; Sembely-Taveau C; Haddad G; Denis C; Soulé N; Suc AL; Listrat A; Toutain A
Am J Med Genet A; 2014 Nov; 164A(11):2926-30. PubMed ID: 25168863
[TBL] [Abstract][Full Text] [Related]
17. [Carpenter syndrome (McK 20100, 20102, 27235)].
Lorenz P; Gedschold J; Hinkel GK; Rupprecht E
Kinderarztl Prax; 1991 Oct; 59(10):317-9. PubMed ID: 1745039
[No Abstract] [Full Text] [Related]
18. Familial occurrence of hemifacial microsomia with radial limb defects.
Moeschler J; Clarren SK
Am J Med Genet; 1982 Aug; 12(4):371-5. PubMed ID: 7124792
[No Abstract] [Full Text] [Related]
19. Impact of communicative disorders on otolaryngologic care of patients with craniofacial anomalies.
Peterson-Falzone SJ
Otolaryngol Clin North Am; 1981 Nov; 14(4):895-915. PubMed ID: 7335363
[No Abstract] [Full Text] [Related]
20. [Mohr's syndrome : type II orofaciodigital syndrome (author's transl)].
Ajacques JC
Rev Stomatol Chir Maxillofac; 1981; 82(4):234-40. PubMed ID: 6269173
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]