Halal F - Search Results

1

Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome.

Halal F, Gledhill R, Dudkiewicz A. Halal F, et al. Am J Med Genet. 1989 Jul;33(3):376-81. doi: 10.1002/ajmg.1320330317. Am J Med Genet. 1989. PMID: 2801772

2

Dominant inheritance of Scheuermann's juvenile kyphosis.

Halal F, Gledhill RB, Fraser C. Halal F, et al. Am J Dis Child. 1978 Nov;132(11):1105-7. doi: 10.1001/archpedi.1978.02120360061011. Am J Dis Child. 1978. PMID: 717319

3

The syndrome of Hirschsprung disease, microcephaly, unusual face, and mental retardation.

Halal F, Morel J. Halal F, et al. Am J Med Genet. 1990 Sep;37(1):106-8. doi: 10.1002/ajmg.1320370125. Am J Med Genet. 1990. PMID: 2240026 Review.

4

Syndrome of microcephaly, Brachmann-de Lange-like facial changes, severe metatarsus adductus, and developmental delay: mild Brachmann-de Lange syndrome?

Halal F, Silver K. Halal F, et al. Am J Med Genet. 1992 Feb 1;42(3):381-6. doi: 10.1002/ajmg.1320420328. Am J Med Genet. 1992. PMID: 1536185

5

Slowly progressive macrocephaly with hamartomas: a new syndrome?

Halal F, Silver K. Halal F, et al. Am J Med Genet. 1989 Jun;33(2):182-5. doi: 10.1002/ajmg.1320330209. Am J Med Genet. 1989. PMID: 2764028

6

Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: a new syndrome.

Der Kaloustian VM, McIntosh N, Silver K, Blaichman S, Halal F. Der Kaloustian VM, et al. Among authors: halal f. Am J Med Genet. 1992 Aug 1;43(6):942-5. doi: 10.1002/ajmg.1320430607. Am J Med Genet. 1992. PMID: 1384331

7

Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?

Chitayat D, Haj-Chahine S, Stalker HJ, Azouz EM, Côté A, Halal F. Chitayat D, et al. Among authors: halal f. Am J Med Genet. 1993 Jan 1;45(1):1-4. doi: 10.1002/ajmg.1320450103. Am J Med Genet. 1993. PMID: 8418638

8

Ring chromosome 4 in a child with duodenal atresia.

Halal F, Vekemans M. Halal F, et al. Am J Med Genet. 1990 Sep;37(1):79-82. doi: 10.1002/ajmg.1320370118. Am J Med Genet. 1990. PMID: 2240048

9

Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20.

Halal F, Chitayat D, Parikh H, Rosenblatt B, Tranchemontagne J, Vekemans M, Potier M. Halal F, et al. Am J Med Genet. 1992 Jun 1;43(3):576-9. doi: 10.1002/ajmg.1320430314. Am J Med Genet. 1992. PMID: 1605251

10

A distinct type of hidrotic ectodermal dysplasia.

Halal F, Setton N, Wang NS. Halal F, et al. Am J Med Genet. 1991 Mar 15;38(4):552-6. doi: 10.1002/ajmg.1320380411. Am J Med Genet. 1991. PMID: 2063897

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