137 related articles for article (PubMed ID: 4370930)
1. Carpenter syndrome--acrocephalopolysyndactyly type II.
Eaton AP; Sommer A; Kontras SB; Sayers MP
Birth Defects Orig Artic Ser; 1974; 10(9):249-60. PubMed ID: 4370930
[No Abstract] [Full Text] [Related]
2. Acrocephalopolysyndactyly, type II (Carpenter syndrome).
Der Kaloustian VM; Sinno AA; Nassar SI
Am J Dis Child; 1972 Nov; 124(5):716-8. PubMed ID: 5085485
[No Abstract] [Full Text] [Related]
3. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
Gnamey D; Farriaux JP
J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
[No Abstract] [Full Text] [Related]
4. Acrocephalopolysyndactyly type IV: a new genetic syndrome in 3 sibs.
Goodman RM; Sternberg M; Shem-Tov Y; Katznelson MB; Hertz M; Rotem Y
Clin Genet; 1979 Mar; 15(3):209-14. PubMed ID: 421359
[No Abstract] [Full Text] [Related]
5. Carpenter syndrome in a patient from Tanzania.
Lodhia J; Rego-Garcia I; Koipapi S; Sadiq A; Msuya D; Spaendonk RV; Hamel B; Dekker M
Am J Med Genet A; 2021 Mar; 185(3):986-989. PubMed ID: 33368989
[TBL] [Abstract][Full Text] [Related]
6. Cerebral malformations in Carpenter syndrome.
Taravath S; Tonsgard JH
Pediatr Neurol; 1993; 9(3):230-4. PubMed ID: 8352858
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Acrocephalopolysyndactyly, type Noack, in a large kindred.
Robinow M; Sorauf TJ
Birth Defects Orig Artic Ser; 1975; 11(5):99-106. PubMed ID: 1240778
[TBL] [Abstract][Full Text] [Related]
9. A new craniodigital syndrome with mental retardation.
Scott CR; Bryant JI; Graham CB
J Pediatr; 1971 Apr; 78(4):658-63. PubMed ID: 4323269
[No Abstract] [Full Text] [Related]
10. A case of Carpenter syndrome diagnosed in a 20-week-old fetus with postmortem examination.
Balci S; Onol B; Eryilmaz M; Haytoglu T
Clin Genet; 1997 Jun; 51(6):412-6. PubMed ID: 9237506
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Acrocephalosyndactyly (ACS) (author's transl)].
Fajardo Carmona AV; Pascual Castroviejo I
An Esp Pediatr; 1975; 8(6):639-50. PubMed ID: 174468
[TBL] [Abstract][Full Text] [Related]
13. [Pfeifer type acrocephalosyndactylia (McK 10160, 18075)].
Lorenz P; Tintschert S; Hinkel GK; Rupprecht E
Kinderarztl Prax; 1991 Nov; 59(11):349-50. PubMed ID: 1758141
[No Abstract] [Full Text] [Related]
14. Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22).
Pfeiffer RA
Clin Genet; 1980 Aug; 18(2):142-6. PubMed ID: 6254701
[TBL] [Abstract][Full Text] [Related]
15. 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]
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. Recessive inheritance of apparent Apert syndrome with polysyndactyly?
Sidhu SS; Deshmukh R
Am J Med Genet; 1988 Sep; 31(1):179-80. PubMed ID: 2851938
[No Abstract] [Full Text] [Related]
18. Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndrome.
Kohn G; Malinger G; el Shawwa R; Scheinfeld A; Tepper R; Ornoy A; Lachman R; Rimoin DL
Am J Med Genet; 1995 Mar; 56(2):132-5. PubMed ID: 7625433
[TBL] [Abstract][Full Text] [Related]
19. Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic facies.
Huson SM; Crowley S; Hall CM; Supramaniam G; Winter RM
Clin Dysmorphol; 1993 Jan; 2(1):20-7. PubMed ID: 8298734
[TBL] [Abstract][Full Text] [Related]
20. [Clinical and genetic contribution to the orofacialdigital syndrome].
Wiemann C; Witkowski R
Padiatr Grenzgeb; 1968; 7(2):85-94. PubMed ID: 4304636
[No Abstract] [Full Text] [Related]
[Next] [New Search]
