PubMed (OMIM) for id: 1644017

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Year	Number of Results
1952	1
1966	2
1978	1
1985	1
1987	1
1990	1
2023	0

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Page 1

Acrocephalosyndactyly, a case with congenital cardiac abnormalities.

OWEN RH. OWEN RH. Br J Radiol. 1952 Feb;25(290):103-6. doi: 10.1259/0007-1285-25-290-103. Br J Radiol. 1952. PMID: 14895920 No abstract available.

[On 2 unusual cases of dyscranio-dysphalangia in siblings (atypical acrocephalosyndactylia and questionable splanchonocystic dysencephalia].

Schönenberg H, Scheidhauer E. Schönenberg H, et al. Monatsschr Kinderheilkd (1902). 1966 May;114(5):322-7. Monatsschr Kinderheilkd (1902). 1966. PMID: 5987027 German. No abstract available.

Carpenter's syndrome: acrocephalopolysyndactyly. An autosomal recessive syndrome.

Temtamy SA. Temtamy SA. J Pediatr. 1966 Jul;69(1):111-20. doi: 10.1016/s0022-3476(66)80368-2. J Pediatr. 1966. PMID: 5935752 No abstract available.

Carpenter syndrome: natural history and clinical spectrum.

Robinson LK, James HE, Mubarak SJ, Allen EJ, Jones KL. Robinson LK, et al. Am J Med Genet. 1985 Mar;20(3):461-9. doi: 10.1002/ajmg.1320200307. Am J Med Genet. 1985. PMID: 3993675

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. Cohen DM, et al. Am J Med Genet. 1987 Oct;28(2):311-24. doi: 10.1002/ajmg.1320280208. Am J Med Genet. 1987. PMID: 3322002 Review.

Carpenter syndrome: marked variability of expression to include the Summitt and Goodman syndromes.

Gershoni-Baruch R. Gershoni-Baruch R. Am J Med Genet. 1990 Feb;35(2):236-40. doi: 10.1002/ajmg.1320350218. Am J Med Genet. 1990. PMID: 2309763

Normal intelligence in two children with Carpenter syndrome.

Frias JL, Felman AH, Rosenbloom AL, Finkelstein SN, Hoyt WF, Hall BD. Frias JL, et al. Am J Med Genet. 1978;2(2):191-9. doi: 10.1002/ajmg.1320020210. Am J Med Genet. 1978. PMID: 263437

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