These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
162 related articles for article (PubMed ID: 3048841)
1. Familial achalasia, microcephaly, and mental retardation. Case report and review of literature. Khalifa MM Clin Pediatr (Phila); 1988 Oct; 27(10):509-12. PubMed ID: 3048841 [TBL] [Abstract][Full Text] [Related]
2. Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive condition. Hernández A; Reynoso MC; Soto F; Quiñones D; Nazará Z; Fragoso R Clin Genet; 1989 Dec; 36(6):456-8. PubMed ID: 2591072 [TBL] [Abstract][Full Text] [Related]
3. Achalasia and microcephaly. Dumars KW; Williams JJ; Steele-Sandlin C Am J Med Genet; 1980; 6(4):309-14. PubMed ID: 7211947 [TBL] [Abstract][Full Text] [Related]
4. Familial achalasia associated with adrenocortical insufficiency, alacrima, and neurological abnormalities. Ehrich E; Aranoff G; Johnson WG Am J Med Genet; 1987 Mar; 26(3):637-44. PubMed ID: 3565479 [TBL] [Abstract][Full Text] [Related]
5. A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures. van Haeringen A; Hurst JA; Savidge R; Baraitser M J Med Genet; 1990 Feb; 27(2):127-9. PubMed ID: 2319580 [TBL] [Abstract][Full Text] [Related]
6. Familial microcephaly with severe neurological deficits: a description of five affected siblings. Gross-Tsur V; Joseph A; Blinder G; Amir N Clin Genet; 1995 Jan; 47(1):33-7. PubMed ID: 7774041 [TBL] [Abstract][Full Text] [Related]
7. [Familial Pitt-Rogers-Danks: two new cases]. Cabrera López JC; Marti Herrero M; Fernández Burriel M; Toledo L; de Andrés-Cofiño R; Orera MA Rev Neurol; 2001 Sep 1-15; 33(5):439-43. PubMed ID: 11727212 [TBL] [Abstract][Full Text] [Related]
8. Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivity. Silengo MC; Bell GL; Biagioli M; Guala A; Bianco R; Strandoni P; De Sario PN; Franceschini P Clin Genet; 1986 Dec; 30(6):481-4. PubMed ID: 3815881 [TBL] [Abstract][Full Text] [Related]
9. Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndrome. Harbord MG; Baraitser M; Wilson J J Med Genet; 1989 Jun; 26(6):397-400. PubMed ID: 2738902 [TBL] [Abstract][Full Text] [Related]
10. Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: a new MCA/MR syndrome? Mégarbané A; Haddad-Zebouni S; Nabbout R; Khoury AH; Traboulsi EI Am J Med Genet; 1999 Mar; 83(2):82-7. PubMed ID: 10190477 [TBL] [Abstract][Full Text] [Related]
11. Four siblings with achalasia, alacrimia and neurological abnormalities in a consanguineous family. Kasirga E; Ozkinay F; Tütüncüoğlu S; Aydoğdu S; Colakoğlu Z; Musoğlu A; Yağci A; Taneli B; Yağci RV Clin Genet; 1996 Jun; 49(6):296-9. PubMed ID: 8884077 [TBL] [Abstract][Full Text] [Related]
12. Familial adrenal insufficiency, achalasia, alacrima, peripheral neuropathy, microcephaly, normal plasma very long chain fatty acids, and normal muscle mitochondrial respiratory chain enzymes. Tsao CY; Romshe CA; Lo WD; Wright FS; Sommer A J Child Neurol; 1994 Apr; 9(2):135-8. PubMed ID: 8006362 [TBL] [Abstract][Full Text] [Related]
13. X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family. Kang WM; Huang CC; Lin SJ Am J Med Genet; 1992 Nov; 44(5):619-23. PubMed ID: 1481821 [TBL] [Abstract][Full Text] [Related]
14. Warburg micro syndrome in two children from a highly inbred Turkish family. Yildirim MS; Zamani AG; Bozkurt B Genet Couns; 2012; 23(2):169-74. PubMed ID: 22876574 [TBL] [Abstract][Full Text] [Related]
15. Evidence of GMPPA founder mutation in indigenous Guatemalan population associated with alacrima, achalasia, and mental retardation syndrome. Diaz J; Kane TD; Leon E Am J Med Genet A; 2020 Mar; 182(3):425-430. PubMed ID: 31898852 [TBL] [Abstract][Full Text] [Related]
16. A possible major contribution to mental retardation in the general population by the gene for microcephaly. Qazi QH; Reed TE Clin Genet; 1975 Feb; 7(2):85-90. PubMed ID: 1132165 [TBL] [Abstract][Full Text] [Related]
17. Achalasia-microcephaly syndrome: a further case report. Wafik M; Kini U Clin Dysmorphol; 2017 Jul; 26(3):190-192. PubMed ID: 28471776 [No Abstract] [Full Text] [Related]
18. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome. Nevin NC; Thomas PS; Hutchinson J Am J Med Genet; 1986 May; 24(1):33-9. PubMed ID: 3706411 [TBL] [Abstract][Full Text] [Related]
19. Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2). Sutherland GR; Gedeon AK; Haan EA; Woodroffe P; Mulley JC Am J Med Genet; 1988; 30(1-2):493-508. PubMed ID: 3177467 [TBL] [Abstract][Full Text] [Related]
20. An X-linked syndrome with microcephaly, severe mental retardation, spasticity, epilepsy and deafness. Renier WO; Gabreëls FJ; Jasper HH; Hustinx TW; Geelen JA; van Haelst UJ J Ment Defic Res; 1982 Mar; 26(Pt 1):27-40. PubMed ID: 7077653 [No Abstract] [Full Text] [Related] [Next] [New Search]