F. Halal

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A new syndrome of severe upper limb hypoplasia and Müllerian duct anomalies.

F. Halal, 1986, American journal of medical genetics.

Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3.

D. Cole, C. Scriver, T. Costa, 1981, Archives of disease in childhood.

Autosomal hypophosphataemic bonedisease responds

D. Cole, C. Scriver, T. Costa, 1981 .

Male to male transmission of cerebral gigantism.

F. Halal, 1982, American journal of medical genetics.

Cerebral gigantism, intestinal polyposis, and pigmentary spotting of the genitalia.

F. Halal, 1983, American journal of medical genetics.

Intracranial aneurysms: a report of a large pedigree.

F. Halal, G. Mohr, T. Toussi, 1983, American journal of medical genetics.

Differential diagnosis in young women with oligomenorrhea and the pseudo-pseudohypoparathyroidism variant of Albright's hereditary osteodystrophy.

F. Halal, C. van Dop, J. Lord, 1985, American journal of medical genetics.

Generalized enchondromatosis in a boy with only platyspondyly in the father.

F. Halal, E. Azouz, 1991, American journal of medical genetics.

The hand-foot-genital (hand-foot-uterus) syndrome: family report and update.

J. Opitz, F. Halal, J. Reynolds, 1988, American journal of medical genetics.

Prevalence of hypomineralised second primary molars (HSPM) in Syrian preschool children

F. Halal, N. Raslan, 2020, European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry.

Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.

Fraser Fc, J. Sproule, F. Fraser, 1980, American journal of medical genetics.

Ruvalcaba‐Myhre‐Smith Syndrome

B. Blumberg, J. Diliberti, R. Weleber, 1988, Pediatric dermatology.

Gastro-cutaneous syndrome: peptic ulcer/hiatal hernia, multiple lentigines/café-au-lait spots, hypertelorism, and myopia.

R. Lesage, F. Halal, M. Gervais, 1982, American journal of medical genetics.

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

K. Silver, F. Halal, 1992, American journal of medical genetics.

The hand profile on de Lange syndrome: diagnostic criteria.

F. Halal, M. Preus, 1979, American journal of medical genetics.

Congenital vesicular eruption caused by Haemophilus influenzae type b.

F. Halal, G. Ahronheim, L. Delorme, 1978, Pediatrics.

Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.

F. Halal, G. Perreault, M. Homsy, 1984, American journal of medical genetics.

Differential diagnosis of Nager acrofacial dysostosis syndrome: report of four patients with Nager syndrome and discussion of other related syndromes.

J. Opitz, F. Halal, P. Pallister, 1983, American journal of medical genetics.

Distal obstructive uropathy with polydactyly: a new syndrome?

F. Halal, 1986, American journal of medical genetics.

Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.

Stephen R. Williams, V. D. Der Kaloustian, H. Toriello, 2010, American journal of human genetics.

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

V. D. Der Kaloustian, K. Silver, F. Halal, 1992, American journal of medical genetics.

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

F. Halal, A. Dudkiewicz, R. Gledhill, 1989, American journal of medical genetics.

PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implications.

E. Lemyre, L. Armstrong, F. Tihy, 2019, Cancer genetics.

A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q.

M. Vekemans, V. D. Der Kaloustian, F. Halal, 1989, American journal of medical genetics.

Minor manifestations in preaxial polydactyly type 1 and Poland complex.

F. Halal, 1981, American journal of medical genetics.

Dominant inheritance of nose pits

J. Opitz, F. Halal, M. Desgranges, 1982 .

Clinical and genetic aspects of antithrombin III deficiency.

F. Halal, S. Laurin, G. Quenneville, 1983, American journal of medical genetics.

Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome?

S. Aymé, J. Sproule, F. Fraser, 1983, American journal of medical genetics.

Acro-renal-mandibular syndrome.

F. Halal, M. Desgranges, B. Leduc, 1980, American journal of medical genetics.

Interstitial tandem direct duplication of the long arm of chromosome 4 (q23-q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segment.

D. Chitayat, M. Vekemans, F. Halal, 1991, American journal of medical genetics.

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

F. Halal, J. Morel, 1990, American journal of medical genetics.

Dominant inheritance of Scheuermann's juvenile kyphosis.

F. Halal, R. Gledhill, C. Fraser, 1978, American journal of diseases of children.

A distinct type of hidrotic ectodermal dysplasia.

F. Halal, N. Wang, N. Setton, 1991, American journal of medical genetics.

Dominant inheritance of acromial skin dimples

J. Opitz, F. Halal, 1980 .

Slowly progressive macrocephaly with hamartomas: a new syndrome?

K. Silver, F. Halal, 1989, American journal of medical genetics.

Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations

A. Rump, A. Verloes, N. Donato, 2013, European Journal of Human Genetics.

Cystathioninuria, renal iminoglycinuria and...alpha 1-antitrypsin...deficiency in the same family: relevance in medical practice.

D. Cox, C. Scriver, F. Halal, 1979, Canadian Medical Association journal.

Ring chromosome 4 in a child with duodenal atresia.

M. Vekemans, F. Halal, 1990, American journal of medical genetics.

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.

B. Rosenblatt, D. Chitayat, M. Vekemans, 1992, American journal of medical genetics.

Monozygotic twins discordant for fibular aplasia.

F. Halal, 1991, American journal of medical genetics.

Brief clinical report: renal hypodysplasia and unilateral ovarian agenesis in the penta-X syndrome.

J. Opitz, R. Lesage, F. Halal, 1980, American journal of medical genetics.

Distal deletion of chromosome 1q in an adult.

P. Kaplan, M. Vekemans, S. Zeesman, 1990, American journal of medical genetics.

[Anterior urethral valve in a newborn infant].

F. Halal, Y. Homsy, I. Laberge, 1979, Canadian Medical Association journal.

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

D. Chitayat, H. Stalker, F. Halal, 1993, American journal of medical genetics.

Severe disseminated lung disease and bronchiectasis probably due to Mycoplasma pneumoniae.

G. Delage, F. Halal, P. Brochu, 1977, Canadian Medical Association journal.

Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly.

F. Halal, P. D. de Bosset, D. Raymond-Tremblay, 1982, American journal of medical genetics.

Dermatoglyphics in dup(4p15→4pter) syndrome

F. Halal, M. Katznelson, 1983 .